A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634788



Internal ID6674903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:66577801..66681072hg38UCSC Ensembl
chr14:67044519..67147790hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38103272
hg19103272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15046046, essv15046045
SamplesHG02895, HG03717
Known GenesGPHN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634788
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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