A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3501647



Internal ID18799928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5623495..5675162hg38UCSC Ensembl
Innerchr10:5665458..5717125hg19UCSC Ensembl
Innerchr10:5705464..5757131hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3851668
hg1951668
hg1851668
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052519
Supporting Variants
Samples
Known GenesASB13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3501647
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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