A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586106



Internal ID16026829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45575897..45582884hg38UCSC Ensembl
Innerchr20:44204536..44211523hg19UCSC Ensembl
Innerchr20:43637950..43644937hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg386988
hg196988
hg186988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7589n54
Supporting Variantsnssv940819
Samples
Known GenesWFDC8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586106
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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