A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621296



Internal ID6661475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102862345..103012326hg38UCSC Ensembl
chr9:105624627..105774608hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38149982
hg19149982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13588134
SamplesHG01485
Known GenesCYLC2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621296
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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