A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643165



Internal ID7029934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76218707..76226810hg38UCSC Ensembl
Innerchr18:76218707..76226810hg38UCSC Ensembl
Outerchr18:76218645..76226868hg38UCSC Ensembl
chr18:73930662..73938765hg19UCSC Ensembl
Innerchr18:73930662..73938765hg19UCSC Ensembl
Outerchr18:73930600..73938823hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg388104
hg198104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv641e214
Supporting Variantsessv15937342, essv15937340, essv15937341
SamplesNA06984, HG03061, NA18488
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643165
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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