A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562708



Internal ID16350117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91348005..91349044hg38UCSC Ensembl
Innerchr13:92000259..92001298hg19UCSC Ensembl
Innerchr13:90798260..90799299hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381040
hg191040
hg181040
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3316n54
Supporting Variantsnssv817448
Samples
Known GenesMIR17HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562708
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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