A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637526



Internal ID6677630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101795171..101829071hg38UCSC Ensembl
chr15:102335374..102369274hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3833901
hg1933901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv470e214
Supporting Variantsessv15354540, essv15354541
SamplesHG00121, NA20797
Known GenesOR4F15, OR4F6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637526
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