A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641476



Internal ID6681561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:168431..177684hg38UCSC Ensembl
Innerchr18:168931..177184hg38UCSC Ensembl
Outerchr18:167431..178684hg38UCSC Ensembl
chr18:168431..177684hg19UCSC Ensembl
Innerchr18:168931..177184hg19UCSC Ensembl
Outerchr18:167431..178684hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg389254
hg199254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15771616, essv15771617, essv15771618, essv15771615, essv15771619
SamplesNA19466, HG01503, HG01709, HG01670, HG00732
Known GenesUSP14
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641476
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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