A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620566



Internal ID6660747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69712247..69717695hg38UCSC Ensembl
chr9:72327163..72332611hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg385449
hg195449
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13511550, essv13511551, essv13511552
SamplesNA19461, NA19467, NA19735
Known GenesPTAR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620566
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