A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv937576



Internal ID16231532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7404601..7422162hg38UCSC Ensembl
Innerchr20:7385248..7402809hg19UCSC Ensembl
Innerchr20:7333248..7350809hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3817562
hg1917562
hg1817562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585357
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)nssv937576
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