A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585781



Internal ID16373190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26275929..26337643hg38UCSC Ensembl
Innerchr20:26256565..26318279hg19UCSC Ensembl
Innerchr20:26204565..26266279hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3861715
hg1961715
hg1861715
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7530n54
Supporting Variantsnssv939013, nssv939012, nssv939014, nssv939009, nssv939011, nssv939010
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585781
Frequency
Sample Size17421
Observed Gain5
Observed Loss1
Observed Complex0
Frequencyn/a


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