A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15064590



Internal ID2977464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76062592..76073150hg38UCSC Ensembl
Innerchr14:76062614..76073128hg38UCSC Ensembl
Outerchr14:76062570..76073172hg38UCSC Ensembl
chr14:76528935..76539493hg19UCSC Ensembl
Innerchr14:76528957..76539471hg19UCSC Ensembl
Outerchr14:76528913..76539515hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3810559
hg1910559
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634978
Supporting Variants
SamplesHG02628
Known GenesIFT43
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15064590
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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