A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621853



Internal ID7008719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130110577..130158140hg38UCSC Ensembl
chr9:132872856..132920419hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3847564
hg1947564
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13629228
SamplesHG01524
Known GenesGPR107
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621853
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