A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13407050



Internal ID6280033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13880761..13908489hg38UCSC Ensembl
Innerchr9:13880761..13908489hg38UCSC Ensembl
Outerchr9:13880261..13908989hg38UCSC Ensembl
chr9:13880760..13908488hg19UCSC Ensembl
Innerchr9:13880760..13908488hg19UCSC Ensembl
Outerchr9:13880260..13908988hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3827729
hg1927729
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619743
Supporting Variants
SamplesNA19795
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13407050
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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