A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610272



Internal ID16397681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10678316..10710120hg38UCSC Ensembl
Innerchr8:10535826..10567630hg19UCSC Ensembl
Innerchr8:10573236..10605040hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3831805
hg1931805
hg1831805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11953n54
Supporting Variantsnssv1156586
SamplesHGDP00515
Known GenesC8orf74
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610272
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