A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585964



Internal ID16026687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:38286018..38343306hg38UCSC Ensembl
Innerchr20:36914420..36971709hg19UCSC Ensembl
Innerchr20:36347834..36405123hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3857289
hg1957290
hg1857290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939356
Samples
Known GenesBPI, LOC149684
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585964
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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