A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8696651



Internal ID13731408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39807534..39821232hg38UCSC Ensembl
Innerchr9:39808534..39820232hg38UCSC Ensembl
Outerchr9:39806534..39822232hg38UCSC Ensembl
chr9:41952552..41966250hg19UCSC Ensembl
Innerchr9:41953552..41965250hg19UCSC Ensembl
Outerchr9:41951552..41967250hg19UCSC Ensembl
chr9:41942552..41956250hg18UCSC Ensembl
Innerchr9:41943552..41955250hg18UCSC Ensembl
Outerchr9:41941552..41957250hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3813699
hg1913699
hg1813699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3351128
Supporting Variants
SamplesNA12892
Known GenesKGFLP2, MGC21881
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8696651
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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