A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585690



Internal ID16373099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:19924165..19924434hg38UCSC Ensembl
Innerchr20:19904809..19905078hg19UCSC Ensembl
Innerchr20:19852809..19853078hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38270
hg19270
hg18270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7510n54
Supporting Variantsnssv938774, nssv938777, nssv938775, nssv938776
Samples
Known GenesRIN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585690
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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