A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621533



Internal ID7008401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113118954..113145520hg38UCSC Ensembl
chr9:115881234..115907800hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3826567
hg1926567
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1502e214
Supporting Variantsessv13606665, essv13606666
SamplesNA20911, NA20849
Known GenesFAM225A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621533
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