A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619615



Internal ID7006489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11595197..11623463hg38UCSC Ensembl
Innerchr9:11595197..11623463hg38UCSC Ensembl
Outerchr9:11594697..11623963hg38UCSC Ensembl
chr9:11595197..11623463hg19UCSC Ensembl
Innerchr9:11595197..11623463hg19UCSC Ensembl
Outerchr9:11594697..11623963hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3828267
hg1928267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13403546, essv13403547
SamplesHG02029, HG03028
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619615
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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