A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15106779



Internal ID6018181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98972768..98973477hg38UCSC Ensembl
Innerchr14:98972794..98973452hg38UCSC Ensembl
Outerchr14:98972743..98973503hg38UCSC Ensembl
chr14:99439105..99439814hg19UCSC Ensembl
Innerchr14:99439131..99439789hg19UCSC Ensembl
Outerchr14:99439080..99439840hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38710
hg19710
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635475
Supporting Variants
SamplesNA19430
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15106779
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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