A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229017



Internal ID22371005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122724688..122750547hg38UCSC Ensembl
chr9:125486967..125512826hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3825860
hg1925860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14347651, nssv14347649, nssv14347650
SamplesHG00512, HG00513, HG00514
Known GenesOR1L4, OR1L6
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229017
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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