A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3508898



Internal ID18460493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:110926565..111035401hg38UCSC Ensembl
Innerchr10:112686323..112795159hg19UCSC Ensembl
Innerchr10:112676313..112785149hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38108837
hg19108837
hg18108837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042020
Supporting Variants
Samples
Known GenesRPL13AP6, SHOC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3508898
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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