A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641671



Internal ID7028445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6566136..6571901hg38UCSC Ensembl
Innerchr18:6566136..6571901hg38UCSC Ensembl
Outerchr18:6566067..6571948hg38UCSC Ensembl
chr18:6566135..6571900hg19UCSC Ensembl
Innerchr18:6566135..6571900hg19UCSC Ensembl
Outerchr18:6566066..6571947hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg385766
hg195766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15793094
SamplesHG02003
Known GenesC18orf64
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641671
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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