A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562728



Internal ID16350137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:92490453..92556340hg38UCSC Ensembl
Innerchr13:93142706..93208593hg19UCSC Ensembl
Innerchr13:91940707..92006594hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3865888
hg1965888
hg1865888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817478
Samples
Known GenesGPC5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562728
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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