A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14966167



Internal ID5736976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34893597..34905729hg38UCSC Ensembl
Innerchr14:34894097..34905229hg38UCSC Ensembl
Outerchr14:34892597..34906729hg38UCSC Ensembl
chr14:35362803..35374935hg19UCSC Ensembl
Innerchr14:35363303..35374435hg19UCSC Ensembl
Outerchr14:35361803..35375935hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3812133
hg1912133
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634044
Supporting Variants
SamplesNA19114
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14966167
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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