A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv943864



Internal ID15891134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63737667..63740688hg38UCSC Ensembl
Innerchr20:62369020..62372041hg19UCSC Ensembl
Innerchr20:61839464..61842485hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg383022
hg193022
hg183022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586632
Supporting Variants
Samples
Known GenesLIME1, SLC2A4RG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv943864
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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