A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635468



Internal ID7022267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98568329..98590979hg38UCSC Ensembl
Innerchr14:98568338..98590970hg38UCSC Ensembl
Outerchr14:98568320..98590988hg38UCSC Ensembl
chr14:99034666..99057316hg19UCSC Ensembl
Innerchr14:99034675..99057307hg19UCSC Ensembl
Outerchr14:99034657..99057325hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3822651
hg1922651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15106751, essv15106749, essv15106754, essv15106747, essv15106753, essv15106746, essv15106748, essv15106744, essv15106750, essv15106752, essv15106745, essv15106743, essv15106755
SamplesHG02574, NA19332, HG03091, NA19041, NA19372, HG01882, HG02307, NA19108, NA19019, NA19380, HG03103, HG02679, HG02760
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635468
Frequency
Sample Size2504
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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