A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14232865



Internal ID3884317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90971570..90977194hg38UCSC Ensembl
Innerchr11:90971570..90977194hg38UCSC Ensembl
Outerchr11:90971070..90977694hg38UCSC Ensembl
chr11:90704738..90710362hg19UCSC Ensembl
Innerchr11:90704738..90710362hg19UCSC Ensembl
Outerchr11:90704238..90710862hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg385625
hg195625
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627230
Supporting Variants
SamplesHG03521
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14232865
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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