A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1106248



Internal ID15959434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10083511..10232639hg38UCSC Ensembl
Innerchr8:9941021..10090149hg19UCSC Ensembl
Innerchr8:9978431..10127559hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38149129
hg19149129
hg18149129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610263
Supporting Variants
Samples
Known GenesMSRA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1106248
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