A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15339039



Internal ID5340855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98889994..98966322hg38UCSC Ensembl
chr15:99433223..99509551hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3876329
hg1976329
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637410
Supporting Variants
SamplesNA19063
Known GenesIGF1R
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15339039
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