A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585689



Internal ID16373098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:19924165..19924267hg38UCSC Ensembl
Innerchr20:19904809..19904911hg19UCSC Ensembl
Innerchr20:19852809..19852911hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38103
hg19103
hg18103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938773
Samples
Known GenesRIN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585689
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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