A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15937346



Internal ID3425218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76230297..76262899hg38UCSC Ensembl
Innerchr18:76230347..76262849hg38UCSC Ensembl
Outerchr18:76230247..76262949hg38UCSC Ensembl
chr18:73942252..73974854hg19UCSC Ensembl
Innerchr18:73942302..73974804hg19UCSC Ensembl
Outerchr18:73942202..73974904hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3832603
hg1932603
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643167
Supporting Variants
SamplesHG03061
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15937346
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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