A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13390411



Internal ID2247899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:6745216..6962830hg38UCSC Ensembl
chr9:6745216..6962830hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38217615
hg19217615
Variant TypeCNV gain
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619440
Supporting Variants
SamplesHG02014
Known GenesKDM4C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13390411
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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