A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447888



Internal ID21105441
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 Variantsnssv18176502
Samples
Known GenesOR1L4, OR1L6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447888
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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