A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511357



Internal ID18809638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26601481..26672705hg38UCSC Ensembl
Innerchr10:26890410..26961634hg19UCSC Ensembl
Innerchr10:26930416..27001640hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3871225
hg1971225
hg1871225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044848
Supporting Variants
Samples
Known GenesLINC00202-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3511357
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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