A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620507



Internal ID7007378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43052167..43075523hg38UCSC Ensembl
chr9:66243042..66266398hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3823357
hg1923357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13493772, essv13493770, essv13493769, essv13493767, essv13493771, essv13493768
SamplesHG01054, NA12058, HG03139, HG00641, HG01603, HG01111
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620507
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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