A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448405



Internal ID21105958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104505382..104652916hg38UCSC Ensembl
chr9:107267663..107415197hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38147535
hg19147535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172679
Samples
Known GenesOR13C2, OR13C3, OR13C4, OR13C5, OR13C8, OR13C9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448405
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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