A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938036



Internal ID16231992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:13467249..13592768hg38UCSC Ensembl
Innerchr20:13447896..13573415hg19UCSC Ensembl
Innerchr20:13395896..13521415hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38125520
hg19125520
hg18125520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585436
Supporting Variants
Samples
Known GenesTASP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv938036
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