A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511802



Internal ID18810083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:95091691..95109294hg38UCSC Ensembl
Innerchr10:96851448..96869051hg19UCSC Ensembl
Innerchr10:96841438..96859041hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3817604
hg1917604
hg1817604
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040153
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)nssv3511802
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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