A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv811796



Internal ID16105752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:55329285..55525875hg38UCSC Ensembl
Innerchr13:55903420..56100010hg19UCSC Ensembl
Innerchr13:54801421..54998011hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg38196591
hg19196591
hg18196591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561707
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv811796
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