A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv812341



Internal ID16106297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:61846409..61921624hg38UCSC Ensembl
Innerchr13:62420542..62495757hg19UCSC Ensembl
Innerchr13:61318543..61393758hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3875216
hg1975216
hg1875216
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561871
Supporting Variants
Samples
Known GenesMIR548AN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv812341
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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