A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619874



Internal ID7006748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18356502..18364845hg38UCSC Ensembl
Innerchr9:18356508..18364839hg38UCSC Ensembl
Outerchr9:18356496..18364851hg38UCSC Ensembl
chr9:18356500..18364843hg19UCSC Ensembl
Innerchr9:18356506..18364837hg19UCSC Ensembl
Outerchr9:18356494..18364849hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg388344
hg198344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13415122, essv13415123
SamplesHG02386, HG00766
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619874
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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