A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149454



Internal ID15531327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98303535..98556312hg38UCSC Ensembl
Innerchr13:98955789..99208566hg19UCSC Ensembl
Innerchr13:97753790..98006567hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38252778
hg19252778
hg18252778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562868
Supporting Variants
SamplesHGDP01081
Known GenesFARP1, STK24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149454
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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