A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15114309



Internal ID1499642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103285894..103287702hg38UCSC Ensembl
Innerchr14:103285897..103287699hg38UCSC Ensembl
Outerchr14:103285891..103287705hg38UCSC Ensembl
chr14:103752231..103754039hg19UCSC Ensembl
Innerchr14:103752234..103754036hg19UCSC Ensembl
Outerchr14:103752228..103754042hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381809
hg191809
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635586
Supporting Variants
SamplesHG01377
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15114309
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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