A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621721



Internal ID6661898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124356835..124451634hg38UCSC Ensembl
chr9:127119114..127213913hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3894800
hg1994800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13618677
SamplesNA19676
Known GenesLOC100129034, PSMB7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621721
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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