A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705665



Internal ID15442317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:21856898..21885308hg38UCSC Ensembl
Innerchr2:22079770..22108180hg19UCSC Ensembl
Innerchr2:21933275..21961685hg18UCSC Ensembl
Innerchr2:21991422..22019832hg17UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3828411
hg1928411
hg1828411
hg1728411
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528966
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705665
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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