A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1029111



Internal ID15882297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:38556243..38556868hg38UCSC Ensembl
Innerchr5:38556345..38556970hg19UCSC Ensembl
Innerchr5:38592102..38592727hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38626
hg19626
hg18626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597858
Supporting Variants
Samples
Known GenesLIFR, LIFR-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1029111
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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