A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1032086



Internal ID15885272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:124355190..124415394hg38UCSC Ensembl
Innerchr5:123690883..123751087hg19UCSC Ensembl
Innerchr5:123718782..123778986hg18UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3860205
hg1960205
hg1860205
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599655
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1032086
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer