A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635309



Internal ID6675422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90382200..90607667hg38UCSC Ensembl
chr14:90848544..91074011hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38225468
hg19225468
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15093258
SamplesNA06984
Known GenesCALM1, LINC00642, TTC7B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635309
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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