A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619471



Internal ID7006345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:7821327..7823470hg38UCSC Ensembl
Innerchr9:7821330..7823467hg38UCSC Ensembl
Outerchr9:7821324..7823473hg38UCSC Ensembl
chr9:7821327..7823470hg19UCSC Ensembl
Innerchr9:7821330..7823467hg19UCSC Ensembl
Outerchr9:7821324..7823473hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg382144
hg192144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13392192, essv13392191
SamplesHG02561, HG02771
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619471
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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