A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634099



Internal ID7020903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37771374..37779543hg38UCSC Ensembl
Innerchr14:37771374..37779543hg38UCSC Ensembl
Outerchr14:37770874..37780043hg38UCSC Ensembl
chr14:38240579..38248748hg19UCSC Ensembl
Innerchr14:38240579..38248748hg19UCSC Ensembl
Outerchr14:38240079..38249248hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg388170
hg198170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14970164, essv14970165
SamplesHG00177, HG03469
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634099
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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