A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3412825



Internal ID15259784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72345633..72345652hg38UCSC Ensembl
Innerchr9:72345629..72345656hg38UCSC Ensembl
Outerchr9:72345610..72345675hg38UCSC Ensembl
chr9:74960549..74960568hg19UCSC Ensembl
Innerchr9:74960545..74960572hg19UCSC Ensembl
Outerchr9:74960526..74960591hg19UCSC Ensembl
chr9:74150369..74150388hg18UCSC Ensembl
Innerchr9:74150392..74150365hg18UCSC Ensembl
Outerchr9:74150346..74150411hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9643614
SamplesNA19143
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3412825
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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