A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619320



Internal ID6659510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3835755..3836613hg38UCSC Ensembl
Innerchr9:3835755..3836613hg38UCSC Ensembl
Outerchr9:3835505..3836859hg38UCSC Ensembl
chr9:3835755..3836613hg19UCSC Ensembl
Innerchr9:3835755..3836613hg19UCSC Ensembl
Outerchr9:3835505..3836859hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13380765, essv13380764
SamplesNA20799, NA19676
Known GenesGLIS3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619320
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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