A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv981187



Internal ID16275143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:166526418..166639778hg38UCSC Ensembl
Innerchr3:166244206..166357566hg19UCSC Ensembl
Innerchr3:167726900..167840260hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38113361
hg19113361
hg18113361
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592486
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv981187
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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