A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1105886



Internal ID15612386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:8240557..8597021hg38UCSC Ensembl
Innerchr8:8098079..8454531hg19UCSC Ensembl
Innerchr8:8135489..8491941hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38356465
hg19356453
hg18356453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610153
Supporting Variants
Samples
Known GenesFAM86B3P, SGK223
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1105886
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