A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1117336



Internal ID15970522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83836704..83895280hg38UCSC Ensembl
Innerchr8:84748939..84807515hg19UCSC Ensembl
Innerchr8:84911494..84970070hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3858577
hg1958577
hg1858577
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611645
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)nssv1117336
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