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nsv5563811

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 167 SVs from 31 studies. See in: genome view    
Submitted genomic39,783,529-39,783,580Question Mark
Overlapping variant regions from other studies: 167 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):40,249,201-40,249,252Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5563811Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr139,783,52939,783,580
nsv5563811RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr140,249,20140,249,252

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16901657sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16901657Submitted genomicNC_000001.11:g.397
83529_39783580ins1
240
GRCh38 (hg38)NC_000001.11Chr139,783,52939,783,580
nssv16901657RemappedPerfectNC_000001.10:g.402
49201_40249252ins1
240
GRCh37.p13First PassNC_000001.10Chr140,249,20140,249,252

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16901657<0.00116404
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