A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635470



Internal ID7022269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98711659..98727377hg38UCSC Ensembl
Innerchr14:98711690..98727346hg38UCSC Ensembl
Outerchr14:98711628..98727408hg38UCSC Ensembl
chr14:99177996..99193714hg19UCSC Ensembl
Innerchr14:99178027..99193683hg19UCSC Ensembl
Outerchr14:99177965..99193745hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3815719
hg1915719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv419e214
Supporting Variantsessv15106758, essv15106762, essv15106757, essv15106763, essv15106760, essv15106759, essv15106761, essv15106764
SamplesHG01066, NA20752, HG01325, HG01064, NA20811, HG00250, HG01697, HG01631
Known GenesC14orf177
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635470
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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