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nsv7097331

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:1,991,842
  • Description:NC_000006.11:g.(?_42162409)_(44154249_?)del AND not provided

Genome View

Select assembly:
Overlapping variant regions from other studies: 5393 SVs from 96 studies. See in: genome view    
Remapped(Score: Perfect):42,194,671-44,186,512Question Mark
Overlapping variant regions from other studies: 5393 SVs from 96 studies. See in: genome view    
Submitted genomic42,162,409-44,154,249Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv7097331RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr642,194,67144,186,512
nsv7097331Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr642,162,40944,154,249

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv18792091deletionMultipleMultiplenot providedUncertain significanceClinVarRCV003107587.2, VCV002424354.3

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv18792091RemappedPerfectNC_000006.12:g.(?_
42194671)_(4418651
2_?)del
GRCh38.p12First PassNC_000006.12Chr642,194,67144,186,512
nssv18792091Submitted genomicNC_000006.11:g.(?_
42162409)_(4415424
9_?)del
GRCh37 (hg19)NC_000006.11Chr642,162,40944,154,249

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDHGVSTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar ID
nssv18792091GRCh37: NC_000006.11:g.(?_42162409)_(44154249_?)deldeletiongermlinenot providedUncertain significanceClinVarRCV003107587.2, VCV002424354.3

No genotype data were submitted for this variant

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