A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv944146



Internal ID16238102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64048115..64049464hg38UCSC Ensembl
Innerchr20:62679468..62680817hg19UCSC Ensembl
Innerchr20:62149912..62151261hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381350
hg191350
hg181350
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586724
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)nssv944146
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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