A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635075



Internal ID6675189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:80712926..80846042hg38UCSC Ensembl
chr14:81179270..81312386hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38133117
hg19133117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15077006
SamplesNA06984
Known GenesCEP128
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635075
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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