A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636106



Internal ID7022902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34238802..34242941hg38UCSC Ensembl
chr15:34531003..34535142hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg384140
hg194140
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15210468, essv15210465, essv15210469, essv15210464, essv15210467, essv15210466
SamplesHG00384, HG03052, NA11933, HG03061, HG03112, HG02186
Known GenesSLC12A6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636106
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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