A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15106745



Internal ID2905469
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635468
Supporting Variants
SamplesHG02574
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15106745
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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