A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv819676



Internal ID16113632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:108767490..109327122hg38UCSC Ensembl
Innerchr13:109419838..109979470hg19UCSC Ensembl
Innerchr13:108217839..108777471hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38559633
hg19559633
hg18559633
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563071
Supporting Variants
Samples
Known GenesMYO16, MYO16-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv819676
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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