A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643131



Internal ID7029900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74908939..74920065hg38UCSC Ensembl
Innerchr18:74908939..74920065hg38UCSC Ensembl
Outerchr18:74908749..74920241hg38UCSC Ensembl
chr18:72620895..72632021hg19UCSC Ensembl
Innerchr18:72620895..72632021hg19UCSC Ensembl
Outerchr18:72620705..72632197hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3811127
hg1911127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15934211, essv15934212, essv15934210
SamplesNA06984, HG03061, NA18989
Known GenesZNF407
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643131
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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