A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15804496



Internal ID2276410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10402977..10405465hg38UCSC Ensembl
Innerchr18:10402991..10405451hg38UCSC Ensembl
Outerchr18:10402963..10405479hg38UCSC Ensembl
chr18:10402974..10405462hg19UCSC Ensembl
Innerchr18:10402988..10405448hg19UCSC Ensembl
Outerchr18:10402960..10405476hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg382489
hg192489
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641776
Supporting Variants
SamplesHG02031
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15804496
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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