A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156191



Internal ID15879554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675987..136839412hg38UCSC Ensembl
Innerchr8:137688230..137851655hg19UCSC Ensembl
Innerchr8:137757412..137920837hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38163426
hg19163426
hg18163426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612421
Supporting Variants
SamplesHGDP01386
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156191
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