A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1119767



Internal ID15972953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114433176..114523864hg38UCSC Ensembl
Innerchr8:115445405..115536093hg19UCSC Ensembl
Innerchr8:115514581..115605269hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3890689
hg1990689
hg1890689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611979
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)nssv1119767
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