A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3499142



Internal ID19086783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9480772..9660846hg38UCSC Ensembl
Innerchr10:9522735..9702809hg19UCSC Ensembl
Innerchr10:9562741..9742815hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38180075
hg19180075
hg18180075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039892
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)nssv3499142
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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