A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633770



Internal ID7020576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22960444..22961365hg38UCSC Ensembl
Innerchr14:22960503..22961306hg38UCSC Ensembl
Outerchr14:22960385..22961424hg38UCSC Ensembl
chr14:23429653..23430574hg19UCSC Ensembl
Innerchr14:23429712..23430515hg19UCSC Ensembl
Outerchr14:23429594..23430633hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38922
hg19922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14935058, essv14935057
SamplesHG02375, HG01403
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633770
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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