A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15825825



Internal ID6116452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26991651..26992374hg38UCSC Ensembl
Innerchr18:26991651..26992374hg38UCSC Ensembl
Outerchr18:26991651..26992374hg38UCSC Ensembl
chr18:24571615..24572338hg19UCSC Ensembl
Innerchr18:24571615..24572338hg19UCSC Ensembl
Outerchr18:24571615..24572338hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642033
Supporting Variants
SamplesNA19654
Known GenesCHST9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15825825
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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