A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv943754



Internal ID16237710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63540916..63594155hg38UCSC Ensembl
Innerchr20:62172269..62225508hg19UCSC Ensembl
Innerchr20:61642713..61695952hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3853240
hg1953240
hg1853240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586576
Supporting Variants
Samples
Known GenesC20orf195, GMEB2, HELZ2, SRMS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv943754
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