A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15089774



Internal ID6604668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85714943..85735729hg38UCSC Ensembl
Innerchr14:85714943..85735729hg38UCSC Ensembl
Outerchr14:85714443..85736229hg38UCSC Ensembl
chr14:86181287..86202073hg19UCSC Ensembl
Innerchr14:86181287..86202073hg19UCSC Ensembl
Outerchr14:86180787..86202573hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3820787
hg1920787
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635201
Supporting Variants
SamplesNA20773
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15089774
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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