A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15817880



Internal ID2861397
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641923
Supporting Variants
SamplesHG02537
Known GenesLOC644669
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15817880
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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