A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990694



Internal ID12624775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:190636465..190870563hg38UCSC Ensembl
Innerchr3:190354254..190588352hg19UCSC Ensembl
Innerchr3:191836948..192071046hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38234099
hg19234099
hg18234099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34194
Supporting Variants
Samples
Known GenesGMNC, IL1RAP
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)essv6990694
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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