A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15105398



Internal ID3162991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98205184..98222742hg38UCSC Ensembl
Innerchr14:98205184..98222742hg38UCSC Ensembl
Outerchr14:98204989..98222923hg38UCSC Ensembl
chr14:98671521..98689079hg19UCSC Ensembl
Innerchr14:98671521..98689079hg19UCSC Ensembl
Outerchr14:98671326..98689260hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3817559
hg1917559
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635459
Supporting Variants
SamplesHG02784
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15105398
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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