A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635497



Internal ID7022296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100176310..100195956hg38UCSC Ensembl
Innerchr14:100176361..100195905hg38UCSC Ensembl
Outerchr14:100176259..100196007hg38UCSC Ensembl
chr14:100642647..100662293hg19UCSC Ensembl
Innerchr14:100642698..100662242hg19UCSC Ensembl
Outerchr14:100642596..100662344hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3819647
hg1919647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15107813
SamplesHG03887
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635497
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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