A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14046194



Internal ID949358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19655426..19663918hg38UCSC Ensembl
Innerchr11:19655426..19663918hg38UCSC Ensembl
Outerchr11:19655156..19664202hg38UCSC Ensembl
chr11:19676972..19685464hg19UCSC Ensembl
Innerchr11:19676972..19685464hg19UCSC Ensembl
Outerchr11:19676702..19685748hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg388493
hg198493
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625539
Supporting Variants
SamplesHG00581
Known GenesNAV2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14046194
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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