A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562722



Internal ID16350131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91955120..92081731hg38UCSC Ensembl
Innerchr13:92607374..92733984hg19UCSC Ensembl
Innerchr13:91405375..91531985hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38126612
hg19126611
hg18126611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817474
Samples
Known GenesGPC5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562722
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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