A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634926



Internal ID7021726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73967124..73979128hg38UCSC Ensembl
Innerchr14:73967124..73979128hg38UCSC Ensembl
Outerchr14:73966624..73979628hg38UCSC Ensembl
chr14:74433827..74445831hg19UCSC Ensembl
Innerchr14:74433827..74445831hg19UCSC Ensembl
Outerchr14:74433327..74446331hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3812005
hg1912005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15060891
SamplesHG03945
Known GenesENTPD5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634926
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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