A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058357



Internal ID18800888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33413503..33558912hg38UCSC Ensembl
Innerchr20:32001309..32146718hg19UCSC Ensembl
Innerchr20:31464970..31610379hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38145410
hg19145410
hg18145410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4302n100
Supporting Variantsnssv3584741, nssv3584740
Samples
Known GenesCBFA2T2, SNTA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058357
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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