A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585956



Internal ID16373365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37358250..37414503hg38UCSC Ensembl
Innerchr20:35986653..36042906hg19UCSC Ensembl
Innerchr20:35420067..35476320hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3856254
hg1956254
hg1856254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939352
Samples
Known GenesSRC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585956
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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