A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562724



Internal ID16350133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:92065477..92093163hg38UCSC Ensembl
Innerchr13:92717730..92745416hg19UCSC Ensembl
Innerchr13:91515731..91543417hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3827687
hg1927687
hg1827687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817475
Samples
Known GenesGPC5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562724
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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