A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv819944



Internal ID15767214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:111063639..111122521hg38UCSC Ensembl
Innerchr13:111715986..111774868hg19UCSC Ensembl
Innerchr13:110513987..110572869hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3858883
hg1958883
hg1858883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563182
Supporting Variants
Samples
Known GenesARHGEF7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv819944
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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