A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635400



Internal ID6675513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95324080..95552963hg38UCSC Ensembl
chr14:95790417..96019300hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38228884
hg19228884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15103388, essv15103389, essv15103390
SamplesHG01052, NA06984, NA19309
Known GenesGLRX5, LINC00341, SCARNA13, SNHG10, SYNE3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635400
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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