A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619322



Internal ID7006200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3934397..3935415hg38UCSC Ensembl
Innerchr9:3934447..3935365hg38UCSC Ensembl
Outerchr9:3934338..3935474hg38UCSC Ensembl
chr9:3934397..3935415hg19UCSC Ensembl
Innerchr9:3934447..3935365hg19UCSC Ensembl
Outerchr9:3934338..3935474hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg381019
hg191019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13380767
SamplesNA19982
Known GenesGLIS3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619322
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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