A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv944140



Internal ID16238096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64047196..64048926hg38UCSC Ensembl
Innerchr20:62678549..62680279hg19UCSC Ensembl
Innerchr20:62148993..62150723hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381731
hg191731
hg181731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586720
Supporting Variants
Samples
Known GenesSOX18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv944140
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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