A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv943871



Internal ID15891141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63737808..63739289hg38UCSC Ensembl
Innerchr20:62369161..62370642hg19UCSC Ensembl
Innerchr20:61839605..61841086hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381482
hg191482
hg181482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586635
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)nssv943871
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer