A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1030368



Internal ID15536868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:55991382..56038098hg38UCSC Ensembl
Innerchr5:55287210..55333925hg19UCSC Ensembl
Innerchr5:55322967..55369682hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3846717
hg1946716
hg1846716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598182
Supporting Variants
Samples
Known GenesFLJ31104, IL6ST
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1030368
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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