A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619411



Internal ID6659600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6620055..6757858hg38UCSC Ensembl
chr9:6620055..6757858hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38137804
hg19137804
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13388021, essv13388022, essv13388020, essv13388019
SamplesNA19795, HG00109, NA19654, NA19756
Known GenesGLDC, KDM4C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619411
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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