A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634927



Internal ID7021727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73968884..73993503hg38UCSC Ensembl
chr14:74435587..74460206hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3824620
hg1924620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15060892, essv15060893, essv15060894
SamplesHG03945, NA19321, NA19439
Known GenesENTPD5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634927
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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