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nsv510961

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:45,688

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 661 SVs from 92 studies. See in: genome view    
Remapped(Score: Perfect):65,451,516-65,497,203Question Mark
Overlapping variant regions from other studies: 675 SVs from 92 studies. See in: genome view    
Remapped(Score: Perfect):64,916,429-64,962,116Question Mark
Overlapping variant regions from other studies: 46 SVs from 9 studies. See in: genome view    
Submitted genomic64,360,579-64,406,266Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv510961RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr765,451,51665,497,203
nsv510961RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr764,916,42964,962,116
nsv510961Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000007.11Chr764,360,57964,406,266

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationOther Calls in this Sample and Study
nssv618657complex substitutionCHMOptical mappingOptical mappingHydatidiform Molenot providedSubmitter1,350

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv618657RemappedPerfectGRCh38.p12First PassNC_000007.14Chr765,451,51665,497,203
nssv618657RemappedPerfectGRCh37.p13First PassNC_000007.13Chr764,916,42964,962,116
nssv618657Submitted genomicNCBI35 (hg17)NC_000007.11Chr764,360,57964,406,266

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDSample IDTypeSubject PhenotypeClinical InterpretationSource of InterpretationGenderOther Calls in this Sample and Study
nssv618657CHMcomplex substitutionHydatidiform Molenot providedSubmitterFemale1,350

No genotype data were submitted for this variant

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