A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635116



Internal ID7021916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:82827775..82836544hg38UCSC Ensembl
Innerchr14:82827802..82836518hg38UCSC Ensembl
Outerchr14:82827749..82836571hg38UCSC Ensembl
chr14:83294119..83302888hg19UCSC Ensembl
Innerchr14:83294146..83302862hg19UCSC Ensembl
Outerchr14:83294093..83302915hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg388770
hg198770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15083040
SamplesHG01799
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635116
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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