A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637480



Internal ID6677584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100508357..100603781hg38UCSC Ensembl
chr15:101048562..101143986hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3895425
hg1995425
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15352169, essv15352171, essv15352170
SamplesNA20861, HG03914, HG04093
Known GenesASB7, CERS3, LINS, PRKXP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637480
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