A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643108



Internal ID7029877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74115165..74123621hg38UCSC Ensembl
Innerchr18:74115193..74123593hg38UCSC Ensembl
Outerchr18:74115137..74123649hg38UCSC Ensembl
chr18:71782400..71790856hg19UCSC Ensembl
Innerchr18:71782428..71790828hg19UCSC Ensembl
Outerchr18:71782372..71790884hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg388457
hg198457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15934059, essv15934058, essv15934057
SamplesHG01632, NA06984, HG03061
Known GenesFBXO15
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643108
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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