A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1047057



Internal ID15900243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:180917407..180981830hg38UCSC Ensembl
Innerchr5:180344407..180408830hg19UCSC Ensembl
Innerchr5:180277013..180341436hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3864424
hg1964424
hg1864424
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600682
Supporting Variants
Samples
Known GenesBTNL8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1047057
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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