A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620353



Internal ID7007224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34192715..34197830hg38UCSC Ensembl
Innerchr9:34192716..34197829hg38UCSC Ensembl
Outerchr9:34192714..34197831hg38UCSC Ensembl
chr9:34192713..34197828hg19UCSC Ensembl
Innerchr9:34192714..34197827hg19UCSC Ensembl
Outerchr9:34192712..34197829hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg385116
hg195116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13458102
SamplesHG02385
Known GenesUBAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620353
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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