A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150972



Internal ID15876821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63540916..63591039hg38UCSC Ensembl
Innerchr20:62172269..62222392hg19UCSC Ensembl
Innerchr20:61642713..61692836hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3850124
hg1950124
hg1850124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586575
Supporting Variants
SamplesHGDP00899
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)nssv1150972
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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