A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585953



Internal ID16026676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37248607..37362389hg38UCSC Ensembl
Innerchr20:35877010..35990792hg19UCSC Ensembl
Innerchr20:35310424..35424206hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38113783
hg19113783
hg18113783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv939350
Samples
Known GenesGHRH, MANBAL, SRC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585953
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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