A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3446057



Internal ID15293007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26052..28950hg38UCSC Ensembl
Innerchr9:27052..27950hg38UCSC Ensembl
Outerchr9:25052..29950hg38UCSC Ensembl
chr9:26052..28950hg19UCSC Ensembl
Innerchr9:27052..27950hg19UCSC Ensembl
Outerchr9:25052..29950hg19UCSC Ensembl
chr9:16052..18950hg18UCSC Ensembl
Innerchr9:17052..17950hg18UCSC Ensembl
Outerchr9:15052..19950hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg382899
hg192899
hg182899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8696612
SamplesNA12892
Known GenesWASH1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3446057
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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