A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13403422



Internal ID2273368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11347309..11623122hg38UCSC Ensembl
Innerchr9:11347327..11623104hg38UCSC Ensembl
Outerchr9:11347291..11623140hg38UCSC Ensembl
chr9:11347309..11623122hg19UCSC Ensembl
Innerchr9:11347327..11623104hg19UCSC Ensembl
Outerchr9:11347291..11623140hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38275814
hg19275814
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619599
Supporting Variants
SamplesHG02029
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13403422
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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