A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3519717



Internal ID18817998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:108997913..109063325hg38UCSC Ensembl
Innerchr10:110757671..110823083hg19UCSC Ensembl
Innerchr10:110747661..110813073hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3865413
hg1965413
hg1865413
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048918
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)nssv3519717
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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