A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611815



Internal ID16399224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:101096809..101119512hg38UCSC Ensembl
Innerchr8:102109037..102131740hg19UCSC Ensembl
Innerchr8:102178213..102200916hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3822704
hg1922704
hg1822704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156142
SamplesHGDP00772
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611815
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