A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585754



Internal ID16373163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25805665..25884215hg38UCSC Ensembl
Innerchr20:25786301..25864851hg19UCSC Ensembl
Innerchr20:25734301..25812851hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3878551
hg1978551
hg1878551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7522n54
Supporting Variantsnssv938983
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585754
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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