A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702284



Internal ID15438936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20562084..20563086hg38UCSC Ensembl
Innerchr10:20851013..20852015hg19UCSC Ensembl
Innerchr10:20891019..20892021hg18UCSC Ensembl
Innerchr10:20891019..20892021hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg381003
hg191003
hg181003
hg171003
Variant TypeCNV gain
Copy Number
Allele State
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)nssv702284
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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