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nsv3960041

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:164,635

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 523 SVs from 59 studies. See in: genome view    
Submitted genomic92,007,078-92,171,712Question Mark
Overlapping variant regions from other studies: 523 SVs from 59 studies. See in: genome view    
Remapped(Score: Perfect):92,400,854-92,565,488Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv3960041Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1292,007,07892,171,712
nsv3960041RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1292,400,85492,565,488

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15209813deletionOptical mappingOptical mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv15209813Submitted genomicNC_000012.12:g.(92
007078_?)_(?_92171
712)del
GRCh38 (hg38)NC_000012.12Chr1292,007,07892,171,712
nssv15209813RemappedPerfectNC_000012.11:g.(92
400854_?)_(?_92565
488)del
GRCh37.p13First PassNC_000012.11Chr1292,400,85492,565,488

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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