A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152497



Internal ID15526110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:87814130..87900583hg38UCSC Ensembl
Innerchr3:87863280..87949733hg19UCSC Ensembl
Innerchr3:87945970..88032423hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3886454
hg1986454
hg1886454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590919
Supporting Variants
SamplesHGDP00041
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152497
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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