A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635320



Internal ID6675433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90887640..90889539hg38UCSC Ensembl
Innerchr14:90887706..90889473hg38UCSC Ensembl
Outerchr14:90887574..90889605hg38UCSC Ensembl
chr14:91353984..91355883hg19UCSC Ensembl
Innerchr14:91354050..91355817hg19UCSC Ensembl
Outerchr14:91353918..91355949hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15094255, essv15094257, essv15094253, essv15094256, essv15094254
SamplesHG03234, HG03709, HG01880, HG03742, HG03871
Known GenesRPS6KA5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635320
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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