A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062082



Internal ID19151301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:763183..928875hg38UCSC Ensembl
Innerchr20:743827..909518hg19UCSC Ensembl
Innerchr20:691827..857518hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38165693
hg19165692
hg18165692
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589963
Samples
Known GenesANGPT4, FAM110A, SLC52A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062082
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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