A curated catalogue of human genomic structural variation




Variant Details

Variant: esv35109



Internal ID12991145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:90138498..90214712hg38UCSC Ensembl
Innerchr8:91150726..91226940hg19UCSC Ensembl
Innerchr8:91219902..91296116hg18UCSC Ensembl
Innerchr8:91219902..91296116hg17UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3876215
hg1976215
hg1876215
hg1776215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6978141, essv6978142, essv6987334
SamplesNA18971
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv35109
Frequency
Sample Size771
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer