A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15934210



Internal ID3425610
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643131
Supporting Variants
SamplesHG03061
Known GenesZNF407
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15934210
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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