A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586355



Internal ID16373764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:58890396..58891803hg38UCSC Ensembl
Innerchr20:57465451..57466858hg19UCSC Ensembl
Innerchr20:56898846..56900253hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg381408
hg191408
hg181408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7625n54
Supporting Variantsnssv941797
Samples
Known GenesGNAS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586355
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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