A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151198



Internal ID15853640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:6306009..6380626hg38UCSC Ensembl
Innerchr20:6286656..6361273hg19UCSC Ensembl
Innerchr20:6234656..6309273hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3874618
hg1974618
hg1874618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585353
Supporting Variants
Samples1780854327_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151198
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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