A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620717



Internal ID7007587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75201604..75358572hg38UCSC Ensembl
chr9:77816520..77973488hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38156969
hg19156969
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13526646, essv13526645
SamplesNA12273, NA19921
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620717
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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