A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153345



Internal ID15875289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:41584977..41596167hg38UCSC Ensembl
Innerchr5:41585079..41596269hg19UCSC Ensembl
Innerchr5:41620836..41632026hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3811191
hg1911191
hg1811191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597880
Supporting Variants
SamplesHGDP00664
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153345
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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