A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990556



Internal ID12624833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:77772218..77793834hg38UCSC Ensembl
Innerchr10:79531976..79553592hg19UCSC Ensembl
Innerchr10:79201982..79223598hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3821617
hg1921617
hg1821617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34173
Supporting Variants
Samples
Known GenesDLG5
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)essv6990556
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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