A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562694



Internal ID16350103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91339903..91348865hg38UCSC Ensembl
Innerchr13:91992157..92001119hg19UCSC Ensembl
Innerchr13:90790158..90799120hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg388963
hg198963
hg188963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3313n54
Supporting Variantsnssv817415
Samples
Known GenesMIR17HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562694
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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