A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562721



Internal ID16350130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91824348..91896587hg38UCSC Ensembl
Innerchr13:92476602..92548841hg19UCSC Ensembl
Innerchr13:91274603..91346842hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3872240
hg1972240
hg1872240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817473
Samples
Known GenesGPC5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562721
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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