A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562715



Internal ID16003438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91409624..91647355hg38UCSC Ensembl
Innerchr13:92061878..92299609hg19UCSC Ensembl
Innerchr13:90859879..91097610hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38237732
hg19237732
hg18237732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3318n54
Supporting Variantsnssv817463
Samples
Known GenesGPC5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562715
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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