A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15936294



Internal ID2718475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76065114..76074433hg38UCSC Ensembl
Innerchr18:76065118..76074429hg38UCSC Ensembl
Outerchr18:76065110..76074437hg38UCSC Ensembl
chr18:73777069..73786388hg19UCSC Ensembl
Innerchr18:73777073..73786384hg19UCSC Ensembl
Outerchr18:73777065..73786392hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg389320
hg199320
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643157
Supporting Variants
SamplesHG02395
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15936294
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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