A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619244



Internal ID7006124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:1181206..1246799hg38UCSC Ensembl
chr9:1181206..1246799hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3865594
hg1965594
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13376794
SamplesHG01353
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619244
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