A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656213



Internal ID15392865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9808205..9813820hg38UCSC Ensembl
Innerchr2:9948334..9953949hg19UCSC Ensembl
Innerchr2:9865785..9871400hg18UCSC Ensembl
Innerchr2:9898932..9904547hg17UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg385616
hg195616
hg185616
hg175616
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517701
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656213
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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