A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643110



Internal ID7029879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74217485..74219846hg38UCSC Ensembl
Innerchr18:74217512..74219820hg38UCSC Ensembl
Outerchr18:74217459..74219873hg38UCSC Ensembl
chr18:71884720..71887081hg19UCSC Ensembl
Innerchr18:71884747..71887055hg19UCSC Ensembl
Outerchr18:71884694..71887108hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg382362
hg192362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15934062
SamplesHG02879
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643110
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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