A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058339



Internal ID19147558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:883869..909706hg38UCSC Ensembl
Innerchr20:864512..890349hg19UCSC Ensembl
Innerchr20:812512..838349hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3825838
hg1925838
hg1825838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589964
Samples
Known GenesANGPT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058339
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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