A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621563



Internal ID7008431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114844006..114847014hg38UCSC Ensembl
Innerchr9:114844017..114847004hg38UCSC Ensembl
Outerchr9:114843996..114847025hg38UCSC Ensembl
chr9:117606286..117609294hg19UCSC Ensembl
Innerchr9:117606297..117609284hg19UCSC Ensembl
Outerchr9:117606276..117609305hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg383009
hg193009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13607919
SamplesNA20801
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621563
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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