A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152525



Internal ID15878166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:110564869..110602188hg38UCSC Ensembl
Innerchr3:110283716..110321035hg19UCSC Ensembl
Innerchr3:111766406..111803725hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3837320
hg1937320
hg1837320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591274
Supporting Variants
SamplesHGDP01103
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152525
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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