A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1047023



Internal ID15553523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179787250..179804248hg38UCSC Ensembl
Innerchr5:179214251..179231248hg19UCSC Ensembl
Innerchr5:179146857..179163854hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3816999
hg1916998
hg1816998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600660
Supporting Variants
Samples
Known GenesLTC4S, MGAT4B, MIR1229
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1047023
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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