A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1154016



Internal ID15881137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:163322967..163369178hg38UCSC Ensembl
Innerchr5:162749973..162796184hg19UCSC Ensembl
Innerchr5:162682551..162728762hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3846212
hg1946212
hg1846212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600189
Supporting Variants
SamplesNINDS_71
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1154016
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