A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620384



Internal ID7007255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35981811..35994247hg38UCSC Ensembl
Innerchr9:35981811..35994247hg38UCSC Ensembl
Outerchr9:35981311..35994747hg38UCSC Ensembl
chr9:35981808..35994244hg19UCSC Ensembl
Innerchr9:35981808..35994244hg19UCSC Ensembl
Outerchr9:35981308..35994744hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3812437
hg1912437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13460284, essv13460283, essv13460282, essv13460281, essv13460285
SamplesHG03074, HG03479, HG03088, HG03039, HG03077
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620384
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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