A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562730



Internal ID16350139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:92556340..92646270hg38UCSC Ensembl
Innerchr13:93208593..93298523hg19UCSC Ensembl
Innerchr13:92006594..92096524hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3889931
hg1989931
hg1889931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817479
Samples
Known GenesGPC5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562730
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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