A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14098162



Internal ID2321716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39082050..39087825hg38UCSC Ensembl
Innerchr11:39082100..39087775hg38UCSC Ensembl
Outerchr11:39082000..39087875hg38UCSC Ensembl
chr11:39103600..39109375hg19UCSC Ensembl
Innerchr11:39103650..39109325hg19UCSC Ensembl
Outerchr11:39103550..39109425hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg385776
hg195776
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626029
Supporting Variants
SamplesHG02067
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14098162
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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