A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634799



Internal ID6674913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:67089063..67105527hg38UCSC Ensembl
Innerchr14:67089063..67105527hg38UCSC Ensembl
Outerchr14:67088685..67105731hg38UCSC Ensembl
chr14:67555780..67572244hg19UCSC Ensembl
Innerchr14:67555780..67572244hg19UCSC Ensembl
Outerchr14:67555402..67572448hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3816465
hg1916465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15046150
SamplesHG02819
Known GenesGPHN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634799
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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