A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15089914



Internal ID2674996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85889713..85953231hg38UCSC Ensembl
Innerchr14:85889713..85953231hg38UCSC Ensembl
Outerchr14:85889213..85953731hg38UCSC Ensembl
chr14:86356057..86419575hg19UCSC Ensembl
Innerchr14:86356057..86419575hg19UCSC Ensembl
Outerchr14:86355557..86420075hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3863519
hg1963519
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635214
Supporting Variants
SamplesHG02371
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15089914
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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