A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672596



Internal ID15062562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3653294..3720485hg38UCSC Ensembl
Innerchr20:3633941..3701132hg19UCSC Ensembl
Innerchr20:3581941..3649132hg18UCSC Ensembl
Innerchr20:3581941..3649132hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3867192
hg1967192
hg1867192
hg1767192
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520565
Supporting Variants
Samples
Known GenesADAM33, GFRA4, SIGLEC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672596
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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