A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15824554



Internal ID636402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26943318..26955016hg38UCSC Ensembl
Innerchr18:26943318..26955016hg38UCSC Ensembl
Outerchr18:26943195..26955144hg38UCSC Ensembl
chr18:24523282..24534980hg19UCSC Ensembl
Innerchr18:24523282..24534980hg19UCSC Ensembl
Outerchr18:24523159..24535108hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3811699
hg1911699
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642029
Supporting Variants
SamplesHG00278
Known GenesCHST9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15824554
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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