A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056394



Internal ID19145613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62436472..62469171hg38UCSC Ensembl
Innerchr20:61011528..61044227hg19UCSC Ensembl
Innerchr20:60444923..60477622hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3832700
hg1932700
hg1832700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584464
Samples
Known GenesGATA5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056394
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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