A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635486



Internal ID7022285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:99605006..99658124hg38UCSC Ensembl
chr14:100071343..100124461hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3853119
hg1953119
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15107086, essv15107088, essv15107087
SamplesNA19457, NA06984, NA19456
Known GenesHHIPL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635486
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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