A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611908



Internal ID16399317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:112946977..113013476hg38UCSC Ensembl
Innerchr8:113959206..114025705hg19UCSC Ensembl
Innerchr8:114028382..114094881hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3866500
hg1966500
hg1866500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156375
SamplesHGDP01337
Known GenesCSMD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611908
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