A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696841



Internal ID15433493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:176883197..176889200hg38UCSC Ensembl
Innerchr5:176310198..176316201hg19UCSC Ensembl
Innerchr5:176242804..176248807hg18UCSC Ensembl
Innerchr5:176242804..176248807hg17UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg386004
hg196004
hg186004
hg176004
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519416
Supporting Variants
Samples
Known GenesHK3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696841
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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