A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15795661



Internal ID5768679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8984577..8985356hg38UCSC Ensembl
Innerchr18:8984627..8985306hg38UCSC Ensembl
Outerchr18:8984527..8985406hg38UCSC Ensembl
chr18:8984575..8985354hg19UCSC Ensembl
Innerchr18:8984625..8985304hg19UCSC Ensembl
Outerchr18:8984525..8985404hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38780
hg19780
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641730
Supporting Variants
SamplesNA19138
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15795661
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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