A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643160



Internal ID7029929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76188333..76194089hg38UCSC Ensembl
Innerchr18:76188352..76194071hg38UCSC Ensembl
Outerchr18:76188315..76194108hg38UCSC Ensembl
chr18:73900288..73906044hg19UCSC Ensembl
Innerchr18:73900307..73906026hg19UCSC Ensembl
Outerchr18:73900270..73906063hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg385757
hg195757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15936303, essv15936304, essv15936305
SamplesNA06984, HG03061, HG03472
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643160
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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