A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635498



Internal ID7022297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100198782..100209301hg38UCSC Ensembl
Innerchr14:100198798..100209286hg38UCSC Ensembl
Outerchr14:100198767..100209317hg38UCSC Ensembl
chr14:100665119..100675638hg19UCSC Ensembl
Innerchr14:100665135..100675623hg19UCSC Ensembl
Outerchr14:100665104..100675654hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3810520
hg1910520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15107814, essv15107815
SamplesHG02614, HG02805
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635498
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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