A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423408



Internal ID21080961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21365598..21390670hg38UCSC Ensembl
chr9:21365597..21390669hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3825073
hg1925073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175764
Samples
Known GenesIFNA13, IFNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423408
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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