A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv816739



Internal ID16110695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:87534417..87621170hg38UCSC Ensembl
Innerchr13:88186672..88273425hg19UCSC Ensembl
Innerchr13:86984673..87071426hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3886754
hg1986754
hg1886754
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562629
Supporting Variants
Samples
Known GenesMIR4500, MIR4500HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv816739
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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