A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14971877



Internal ID886214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37910939..37921835hg38UCSC Ensembl
Innerchr14:37911439..37921335hg38UCSC Ensembl
Outerchr14:37909939..37922835hg38UCSC Ensembl
chr14:38380144..38391040hg19UCSC Ensembl
Innerchr14:38380644..38390540hg19UCSC Ensembl
Outerchr14:38379144..38392040hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3810897
hg1910897
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634105
Supporting Variants
SamplesHG00476
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14971877
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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