A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642224



Internal ID6682305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36318746..36323110hg38UCSC Ensembl
Innerchr18:36318762..36323094hg38UCSC Ensembl
Outerchr18:36318730..36323126hg38UCSC Ensembl
chr18:33898709..33903073hg19UCSC Ensembl
Innerchr18:33898725..33903057hg19UCSC Ensembl
Outerchr18:33898693..33903089hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg384365
hg194365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15842431
SamplesNA18572
Known GenesFHOD3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642224
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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