A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585776



Internal ID16373185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26165527..26265450hg38UCSC Ensembl
Innerchr20:26146163..26246086hg19UCSC Ensembl
Innerchr20:26094163..26194086hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3899924
hg1999924
hg1899924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152381
SamplesHGDP01076
Known GenesLOC284801, MIR663A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585776
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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