A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585678



Internal ID16373087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:19924061..19924216hg38UCSC Ensembl
Innerchr20:19904705..19904860hg19UCSC Ensembl
Innerchr20:19852705..19852860hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38156
hg19156
hg18156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938614, nssv938613
Samples
Known GenesRIN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585678
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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