A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv982903



Internal ID16276859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:188759802..188815021hg38UCSC Ensembl
Innerchr3:188477590..188532809hg19UCSC Ensembl
Innerchr3:189960284..190015503hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3855220
hg1955220
hg1855220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592761
Supporting Variants
Samples
Known GenesLPP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv982903
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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