A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520565



Internal ID15101172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:3652593..3740054hg38UCSC Ensembl
Innerchr20:3633240..3720701hg19UCSC Ensembl
Innerchr20:3581240..3668701hg18UCSC Ensembl
Innerchr20:3581240..3668701hg17UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3887462
hg1987462
hg1887462
hg1787462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv688470, nssv698844, nssv672596
Samples
Known GenesADAM33, GFRA4, HSPA12B, SIGLEC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520565
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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