A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563387



Internal ID16004110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113832338..113876058hg38UCSC Ensembl
Innerchr13:114535311..114579031hg19UCSC Ensembl
Innerchr13:113534912..113578632hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3843721
hg1943721
hg1843721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv820681
Samples
Known GenesGAS6, GAS6-AS1, GAS6-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563387
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer