A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990717



Internal ID12971484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:163877641..163935916hg38UCSC Ensembl
Innerchr1:163846878..163905153hg19UCSC Ensembl
Innerchr1:162113502..162171777hg18UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3858276
hg1958276
hg1858276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34034
Supporting Variants
Samples
Known Genes
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)essv6990717
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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