A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619885



Internal ID7006759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18843033..18858782hg38UCSC Ensembl
Innerchr9:18843533..18858282hg38UCSC Ensembl
Outerchr9:18842033..18859782hg38UCSC Ensembl
chr9:18843031..18858780hg19UCSC Ensembl
Innerchr9:18843531..18858280hg19UCSC Ensembl
Outerchr9:18842031..18859780hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3815750
hg1915750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13415193
SamplesHG02816
Known GenesADAMTSL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619885
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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