A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv820682



Internal ID15767952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113754200..113872798hg38UCSC Ensembl
Innerchr13:114457173..114575771hg19UCSC Ensembl
Innerchr13:113538172..113656958hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38118599
hg19118599
hg18118787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563388
Supporting Variants
Samples
Known GenesGAS6, GAS6-AS1, GAS6-AS2, TMEM255B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv820682
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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