A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688183



Internal ID15424835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20561695..20565639hg38UCSC Ensembl
Innerchr10:20850624..20854568hg19UCSC Ensembl
Innerchr10:20890630..20894574hg18UCSC Ensembl
Innerchr10:20890630..20894574hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg383945
hg193945
hg183945
hg173945
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)nssv688183
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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