A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv940979



Internal ID15888249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:49522434..49559141hg38UCSC Ensembl
Innerchr20:48138971..48175678hg19UCSC Ensembl
Innerchr20:47572378..47609085hg18UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3836708
hg1936708
hg1836708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586173
Supporting Variants
Samples
Known GenesPTGIS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv940979
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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