A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685671



Internal ID15075637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:87811540..87811759hg38UCSC Ensembl
Innerchr4:88732692..88732911hg19UCSC Ensembl
Innerchr4:88951716..88951935hg18UCSC Ensembl
Innerchr4:89089871..89090090hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38220
hg19220
hg18220
hg17220
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515943
Supporting Variants
Samples
Known GenesIBSP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685671
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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