A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641669



Internal ID7028443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6542085..6556192hg38UCSC Ensembl
Innerchr18:6542100..6556177hg38UCSC Ensembl
Outerchr18:6542070..6556207hg38UCSC Ensembl
chr18:6542084..6556191hg19UCSC Ensembl
Innerchr18:6542099..6556176hg19UCSC Ensembl
Outerchr18:6542069..6556206hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3814108
hg1914108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15793092
SamplesHG01046
Known GenesC18orf64
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641669
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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