A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637491



Internal ID7024283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100938303..100955590hg38UCSC Ensembl
chr15:101478508..101495795hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3817288
hg1917288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15353927
SamplesHG00183
Known GenesLRRK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637491
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