A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636057



Internal ID7022853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31606654..31738742hg38UCSC Ensembl
chr15:31898857..32030945hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38132089
hg19132089
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv446e214
Supporting Variantsessv15206661, essv15206658, essv15206657, essv15206660, essv15206659
SamplesNA12287, HG01973, HG00141, NA06986, HG02679
Known GenesOTUD7A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636057
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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