A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150938



Internal ID15507211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:349198..372441hg38UCSC Ensembl
Innerchr20:329842..353085hg19UCSC Ensembl
Innerchr20:277842..301085hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3823244
hg1923244
hg1823244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585168
Supporting Variants
Samples1780854479_A
Known GenesNRSN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150938
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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