A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3492263



Internal ID19079904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2379018..2500647hg38UCSC Ensembl
Innerchr10:2421212..2542839hg19UCSC Ensembl
Innerchr10:2411212..2532839hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38121630
hg19121628
hg18121628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049863
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)nssv3492263
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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