A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15102282



Internal ID3188713
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635369
Supporting Variants
SamplesHG02804
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15102282
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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