A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662990



Internal ID15399642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:163322967..163369178hg38UCSC Ensembl
Innerchr5:162749973..162796184hg19UCSC Ensembl
Innerchr5:162682551..162728762hg18UCSC Ensembl
Innerchr5:162682551..162728762hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3846212
hg1946212
hg1846212
hg1746212
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520335
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662990
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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