A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3494091



Internal ID19081732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2271708..2288795hg38UCSC Ensembl
Innerchr10:2313902..2330989hg19UCSC Ensembl
Innerchr10:2303902..2320989hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3817088
hg1917088
hg1817088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052783
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)nssv3494091
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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