A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153568



Internal ID15877025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:106020189..106062774hg38UCSC Ensembl
Innerchr5:105355890..105398475hg19UCSC Ensembl
Innerchr5:105383789..105426374hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3842586
hg1942586
hg1842586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599283
Supporting Variants
SamplesHGDP00926
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153568
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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