A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3390211



Internal ID14890492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35912992..35914532hg38UCSC Ensembl
Innerchr9:35912992..35914532hg38UCSC Ensembl
Outerchr9:35912718..35914548hg38UCSC Ensembl
chr9:35912989..35914529hg19UCSC Ensembl
Innerchr9:35912989..35914529hg19UCSC Ensembl
Outerchr9:35912715..35914545hg19UCSC Ensembl
chr9:35902989..35904529hg18UCSC Ensembl
Innerchr9:35902989..35904529hg18UCSC Ensembl
Outerchr9:35902715..35904545hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381541
hg191541
hg181541
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8652436
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3390211
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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