A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990726



Internal ID12624807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:33366714..33721288hg38UCSC Ensembl
Innerchr14:33835920..34190494hg19UCSC Ensembl
Innerchr14:32905671..33260245hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38354575
hg19354575
hg18354575
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34178
Supporting Variants
Samples
Known GenesNPAS3
MethodSNP array
AnalysisWe further explored the discovery of segmental deletions in the Kosraean population data where IBD is more prevalent, and we observe a larger number of gaps.We used a binomial score to rank potential deletions in homozygous gaps based on the number of mismatching SNPs and the rate of mismatch in the flanking shared segments, measured across all shared segments with the suspected gap. To prioritize the segmental gaps that were most likely to be representative of a deletion, we developed a scoring function based on the number of mismatching SNPs and levels of homozygosity in the gap.
PlatformNot reported
Comments
ReferenceGusev_et_al_2009
Pubmed ID18971310
Accession Number(s)essv6990726
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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