A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563391



Internal ID16004114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113824151..113825282hg38UCSC Ensembl
Innerchr13:114527124..114528255hg19UCSC Ensembl
Innerchr13:113585688..113586819hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381132
hg191132
hg181132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv820685
Samples
Known GenesGAS6, GAS6-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563391
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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