A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15824599



Internal ID1943584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26980559..26983786hg38UCSC Ensembl
Innerchr18:26980567..26983779hg38UCSC Ensembl
Outerchr18:26980552..26983794hg38UCSC Ensembl
chr18:24560523..24563750hg19UCSC Ensembl
Innerchr18:24560531..24563743hg19UCSC Ensembl
Outerchr18:24560516..24563758hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383228
hg193228
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642032
Supporting Variants
SamplesHG01806
Known GenesCHST9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15824599
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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