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nsv510894

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:21,411

Links to Other Resources

Genome View

Select assembly:
Overlapping variant regions from other studies: 371 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):176,115,537-176,136,947Question Mark
Overlapping variant regions from other studies: 371 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):177,036,688-177,058,098Question Mark
Overlapping variant regions from other studies: 20 SVs from 2 studies. See in: genome view    
Submitted genomic177,411,837-177,433,247Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv510894RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr4176,115,537176,136,947
nsv510894RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4177,036,688177,058,098
nsv510894Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000004.9Chr4177,411,837177,433,247

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationOther Calls in this Sample and Study
nssv618607complex substitutionCHMOptical mappingOptical mappingHydatidiform Molenot providedSubmitter1,350

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv618607RemappedPerfectGRCh38.p12First PassNC_000004.12Chr4176,115,537176,136,947
nssv618607RemappedPerfectGRCh37.p13First PassNC_000004.11Chr4177,036,688177,058,098
nssv618607Submitted genomicNCBI35 (hg17)NC_000004.9Chr4177,411,837177,433,247

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDSample IDTypeSubject PhenotypeClinical InterpretationSource of InterpretationGenderOther Calls in this Sample and Study
nssv618607CHMcomplex substitutionHydatidiform Molenot providedSubmitterFemale1,350

No genotype data were submitted for this variant

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