A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635369



Internal ID7022168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:93881516..93884918hg38UCSC Ensembl
Innerchr14:93881534..93884901hg38UCSC Ensembl
Outerchr14:93881499..93884936hg38UCSC Ensembl
chr14:94347862..94351264hg19UCSC Ensembl
Innerchr14:94347880..94351247hg19UCSC Ensembl
Outerchr14:94347845..94351282hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg383403
hg193403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15102284, essv15102282, essv15102283
SamplesHG02804, NA18977, NA19391
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635369
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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