A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621804



Internal ID6661980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128166528..128179690hg38UCSC Ensembl
Innerchr9:128166528..128179690hg38UCSC Ensembl
Outerchr9:128166028..128180190hg38UCSC Ensembl
chr9:130928807..130941969hg19UCSC Ensembl
Innerchr9:130928807..130941969hg19UCSC Ensembl
Outerchr9:130928307..130942469hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3813163
hg1913163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13622811
SamplesHG03234
Known GenesCIZ1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621804
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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