A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14184864



Internal ID4186680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63691248..63696739hg38UCSC Ensembl
Innerchr11:63691298..63696689hg38UCSC Ensembl
Outerchr11:63691198..63696789hg38UCSC Ensembl
chr11:63458720..63464211hg19UCSC Ensembl
Innerchr11:63458770..63464161hg19UCSC Ensembl
Outerchr11:63458670..63464261hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg385492
hg195492
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626651
Supporting Variants
SamplesHG03844
Known GenesRTN3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14184864
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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