A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14221296



Internal ID6799126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85371245..85383797hg38UCSC Ensembl
Innerchr11:85371248..85383794hg38UCSC Ensembl
Outerchr11:85371242..85383800hg38UCSC Ensembl
chr11:85082289..85094841hg19UCSC Ensembl
Innerchr11:85082292..85094838hg19UCSC Ensembl
Outerchr11:85082286..85094844hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3812553
hg1912553
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3627061
Supporting Variants
SamplesNA20889
Known GenesDLG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14221296
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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