A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700263



Internal ID15436915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:84085822..84293989hg38UCSC Ensembl
Innerchr4:85006975..85215142hg19UCSC Ensembl
Innerchr4:85225999..85434166hg18UCSC Ensembl
Innerchr4:85364154..85572321hg17UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38208168
hg19208168
hg18208168
hg17208168
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524354
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700263
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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