A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15098407



Internal ID2960839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92870142..92871777hg38UCSC Ensembl
Innerchr14:92870192..92871727hg38UCSC Ensembl
Outerchr14:92870092..92871827hg38UCSC Ensembl
chr14:93336487..93338122hg19UCSC Ensembl
Innerchr14:93336537..93338072hg19UCSC Ensembl
Outerchr14:93336437..93338172hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg381636
hg191636
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635347
Supporting Variants
SamplesHG02614
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15098407
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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