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nsv3417491

  • Variant Calls:3
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:68,200

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Submitted genomic78,101-146,500Question Mark
Overlapping variant regions from other studies: 349 SVs from 48 studies. See in: genome view    
Remapped(Score: Good):142,628,636-142,697,063Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv3417491Submitted genomicGRCh38 (hg38)Primary AssemblyNT_187498.1Unplaced|N
T_187498.1
78,201 (-100, +100)146,400 (-100, +100)
nsv3417491RemappedGoodGRCh37.p13Primary AssemblySecond PassNC_000001.10Chr1142,628,736 (-100, +100)142,696,963 (-100, +100)

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv14802746duplicationSAMN09651199Sequencingde novo and local sequence assembly27,381
nssv14803727duplicationSAMN09643900Sequencingde novo and local sequence assembly26,631
nssv14804726duplicationSAMN05181962Sequencingde novo and local sequence assembly23,563

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv14802746Submitted genomicNT_187498.1:g.(781
01_78301)_(146300_
146500)dup
GRCh38 (hg38)NT_187498.1Unplaced|N
T_187498.1
78,201 (-100, +100)146,400 (-100, +100)
nssv14803727Submitted genomicNT_187498.1:g.(781
01_78301)_(146300_
146500)dup
GRCh38 (hg38)NT_187498.1Unplaced|N
T_187498.1
78,201 (-100, +100)146,400 (-100, +100)
nssv14804726Submitted genomicNT_187498.1:g.(781
01_78301)_(146300_
146500)dup
GRCh38 (hg38)NT_187498.1Unplaced|N
T_187498.1
78,201 (-100, +100)146,400 (-100, +100)
nssv14802746RemappedGoodNC_000001.10:g.(14
2628636_142628836)
_(142696863_142697
063)dupNC_000001.1
0:g.(142628636_142
628836)_(142696863
_142697063)dup
GRCh37.p13Second PassNC_000001.10Chr1142,628,736 (-100, +100)142,696,963 (-100, +100)
nssv14803727RemappedGoodNC_000001.10:g.(14
2628636_142628836)
_(142696863_142697
063)dupNC_000001.1
0:g.(142628636_142
628836)_(142696863
_142697063)dup
GRCh37.p13Second PassNC_000001.10Chr1142,628,736 (-100, +100)142,696,963 (-100, +100)
nssv14804726RemappedGoodNC_000001.10:g.(14
2628636_142628836)
_(142696863_142697
063)dupNC_000001.1
0:g.(142628636_142
628836)_(142696863
_142697063)dup
GRCh37.p13Second PassNC_000001.10Chr1142,628,736 (-100, +100)142,696,963 (-100, +100)
Showing 6 of 9

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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