A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14088618



Internal ID6040407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34239569..34240953hg38UCSC Ensembl
Innerchr11:34239619..34240904hg38UCSC Ensembl
Outerchr11:34239520..34241003hg38UCSC Ensembl
chr11:34261116..34262500hg19UCSC Ensembl
Innerchr11:34261166..34262451hg19UCSC Ensembl
Outerchr11:34261067..34262550hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381385
hg191385
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625909
Supporting Variants
SamplesNA19440
Known GenesABTB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14088618
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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