A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653669



Internal ID15390321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20562084..20565668hg38UCSC Ensembl
Innerchr10:20851013..20854597hg19UCSC Ensembl
Innerchr10:20891019..20894603hg18UCSC Ensembl
Innerchr10:20891019..20894603hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg383585
hg193585
hg183585
hg173585
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516763
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653669
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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