A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3714931



Internal ID19013212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18712716..18824655hg38UCSC Ensembl
Innerchr13:19286856..19398795hg19UCSC Ensembl
Innerchr13:18184856..18296795hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38111940
hg19111940
hg18111940
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036175
Supporting Variants
Samples
Known GenesLINC00417
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3714931
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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