A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3485707



Internal ID19073348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1893193..1950452hg38UCSC Ensembl
Innerchr10:1935387..1992646hg19UCSC Ensembl
Innerchr10:1925387..1982646hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3857260
hg1957260
hg1857260
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037341
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3485707
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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