A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152353



Internal ID15508666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:2657933..2704278hg38UCSC Ensembl
Innerchr20:2638579..2684924hg19UCSC Ensembl
Innerchr20:2586579..2632924hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3846346
hg1946346
hg1846346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585266
Supporting Variants
Samples1780862574_A
Known GenesEBF4, IDH3B, NOP56
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152353
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