A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586463



Internal ID16373872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62064568..62066551hg38UCSC Ensembl
Innerchr20:60639624..60641607hg19UCSC Ensembl
Innerchr20:60073019..60075002hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381984
hg191984
hg181984
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7646n54
Supporting Variantsnssv942017, nssv942016, nssv942018, nssv942020, nssv942022, nssv942021, nssv942019
Samples
Known GenesTAF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586463
Frequency
Sample Size17421
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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