A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634645



Internal ID7021448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59383730..59391957hg38UCSC Ensembl
Innerchr14:59383764..59391923hg38UCSC Ensembl
Outerchr14:59383696..59391991hg38UCSC Ensembl
chr14:59850448..59858675hg19UCSC Ensembl
Innerchr14:59850482..59858641hg19UCSC Ensembl
Outerchr14:59850414..59858709hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg388228
hg198228
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15025893, essv15025894, essv15025892
SamplesNA18962, HG00421, HG02013
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634645
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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