A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153569



Internal ID15879318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:106022528..106070173hg38UCSC Ensembl
Innerchr5:105358229..105405874hg19UCSC Ensembl
Innerchr5:105386128..105433773hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3847646
hg1947646
hg1847646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599286
Supporting Variants
SamplesHGDP01345
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153569
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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