A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1122265



Internal ID15975451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675712..136829581hg38UCSC Ensembl
Innerchr8:137687955..137841824hg19UCSC Ensembl
Innerchr8:137757137..137911006hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38153870
hg19153870
hg18153870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612396
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)nssv1122265
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