A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939354



Internal ID15886624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:37507707..37620600hg38UCSC Ensembl
Innerchr20:36136109..36249002hg19UCSC Ensembl
Innerchr20:35569523..35682416hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38112894
hg19112894
hg18112894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585962
Supporting Variants
Samples
Known GenesBLCAP, LINC00489, NNAT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv939354
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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