A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv820160



Internal ID16114116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:112765821..112767388hg38UCSC Ensembl
Innerchr13:113420135..113421702hg19UCSC Ensembl
Innerchr13:112468136..112469703hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381568
hg191568
hg181568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563233
Supporting Variants
Samples
Known GenesATP11A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv820160
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