A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696787



Internal ID15433439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:44384499..44419546hg38UCSC Ensembl
Innerchr3:44425991..44461038hg19UCSC Ensembl
Innerchr3:44400995..44436042hg18UCSC Ensembl
Innerchr3:44400995..44436042hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3835048
hg1935048
hg1835048
hg1735048
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519315
Supporting Variants
Samples
Known GenesTCAIM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696787
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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