A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671102



Internal ID15407754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20494784..20531900hg38UCSC Ensembl
Innerchr10:20783713..20820829hg19UCSC Ensembl
Innerchr10:20823719..20860835hg18UCSC Ensembl
Innerchr10:20823719..20860835hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3837117
hg1937117
hg1837117
hg1737117
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)nssv671102
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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