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nsv3067637

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1
  • Data Source:HUMANGENOME_JCVI

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 342 SVs from 65 studies. See in: genome view    
Remapped(Score: Perfect):195,787,330-195,787,330Question Mark
Overlapping variant regions from other studies: 89 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):157,163-157,163Question Mark
Overlapping variant regions from other studies: 71 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):7,406-7,406Question Mark
Overlapping variant regions from other studies: 72 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):7,406-7,406Question Mark
Overlapping variant regions from other studies: 72 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):7,406-7,406Question Mark
Overlapping variant regions from other studies: 71 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):7,406-7,406Question Mark
Overlapping variant regions from other studies: 71 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):7,406-7,406Question Mark
Overlapping variant regions from other studies: 342 SVs from 65 studies. See in: genome view    
Submitted genomic195,514,201-195,514,201Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv3067637RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3195,787,330195,787,330
nsv3067637RemappedPerfectGRCh38.p12ALT_REF_LOCI_5Second PassNT_187689.1Chr3|NT_18
7689.1		157,163157,163
nsv3067637RemappedPerfectGRCh38.p12ALT_REF_LOCI_6Second PassNT_187690.1Chr3|NT_18
7690.1		7,4067,406
nsv3067637RemappedPerfectGRCh38.p12ALT_REF_LOCI_7Second PassNT_187691.1Chr3|NT_18
7691.1		7,4067,406
nsv3067637RemappedPerfectGRCh38.p12ALT_REF_LOCI_3Second PassNT_187678.1Chr3|NT_18
7678.1		7,4067,406
nsv3067637RemappedPerfectGRCh38.p12ALT_REF_LOCI_4Second PassNT_187688.1Chr3|NT_18
7688.1		7,4067,406
nsv3067637RemappedPerfectGRCh38.p12ALT_REF_LOCI_2Second PassNT_187649.1Chr3|NT_18
7649.1		7,4067,406
nsv3067637Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3195,514,201195,514,201

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysis
nssv14043466insertion1104685124988CuratedCurated

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv14043466RemappedPerfectNT_187678.1:g.7406
_7407ins144		GRCh38.p12Second PassNT_187678.1Chr3|NT_18
7678.1		7,4067,406
nssv14043466RemappedPerfectNT_187688.1:g.7406
_7407ins144		GRCh38.p12Second PassNT_187688.1Chr3|NT_18
7688.1		7,4067,406
nssv14043466RemappedPerfectNT_187690.1:g.7406
_7407ins144		GRCh38.p12Second PassNT_187690.1Chr3|NT_18
7690.1		7,4067,406
nssv14043466RemappedPerfectNT_187691.1:g.7406
_7407ins144		GRCh38.p12Second PassNT_187691.1Chr3|NT_18
7691.1		7,4067,406
nssv14043466RemappedPerfectNT_187689.1:g.1571
63_157164ins144		GRCh38.p12Second PassNT_187689.1Chr3|NT_18
7689.1		157,163157,163
nssv14043466RemappedPerfectNT_187649.1:g.7406
_7407ins144		GRCh38.p12Second PassNT_187649.1Chr3|NT_18
7649.1		7,4067,406
nssv14043466RemappedPerfectNC_000003.12:g.195
787330_195787331in
s144		GRCh38.p12First PassNC_000003.12Chr3195,787,330195,787,330
nssv14043466Submitted genomicNC_000003.11:g.195
514201_195514202in
s144		GRCh37 (hg19)NC_000003.11Chr3195,514,201195,514,201

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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