A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14090114



Internal ID4091930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34891859..34899584hg38UCSC Ensembl
Innerchr11:34891875..34899568hg38UCSC Ensembl
Outerchr11:34891843..34899600hg38UCSC Ensembl
chr11:34913406..34921131hg19UCSC Ensembl
Innerchr11:34913422..34921115hg19UCSC Ensembl
Outerchr11:34913390..34921147hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg387726
hg197726
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625916
Supporting Variants
SamplesNA11992
Known GenesAPIP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14090114
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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