A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562696



Internal ID16350105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91347483..91348382hg38UCSC Ensembl
Innerchr13:91999737..92000636hg19UCSC Ensembl
Innerchr13:90797738..90798637hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38900
hg19900
hg18900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817417, nssv817418
Samples
Known GenesMIR17HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562696
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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