A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635496



Internal ID6675609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100169585..100290965hg38UCSC Ensembl
chr14:100635922..100757302hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38121381
hg19121381
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15107811, essv15107812
SamplesHG01495, NA06984
Known GenesMIR6764, YY1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635496
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer