A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621099



Internal ID6661279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93408196..93450082hg38UCSC Ensembl
Innerchr9:93408696..93449582hg38UCSC Ensembl
Outerchr9:93407196..93451082hg38UCSC Ensembl
chr9:96170478..96212364hg19UCSC Ensembl
Innerchr9:96170978..96211864hg19UCSC Ensembl
Outerchr9:96169478..96213364hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3841887
hg1941887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13560050
SamplesNA20809
Known GenesFAM120AOS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621099
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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