A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641923



Internal ID7028694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:15311666..15328279hg38UCSC Ensembl
Innerchr18:15311666..15328279hg38UCSC Ensembl
Outerchr18:15311166..15328779hg38UCSC Ensembl
chr18:15311665..15328278hg19UCSC Ensembl
Innerchr18:15311665..15328278hg19UCSC Ensembl
Outerchr18:15311165..15328778hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3816614
hg1916614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15817880, essv15817881, essv15817882, essv15817883
SamplesNA19909, NA19315, HG02537, HG03563
Known GenesLOC644669
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641923
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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