A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv943848



Internal ID15891118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63737451..63739060hg38UCSC Ensembl
Innerchr20:62368804..62370413hg19UCSC Ensembl
Innerchr20:61839248..61840857hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381610
hg191610
hg181610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586620
Supporting Variants
Samples
Known GenesLIME1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv943848
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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