A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420254



Internal ID21077807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13944801..13947000hg38UCSC Ensembl
chr9:13944800..13946999hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174908
Samples
Known GenesLINC00583
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420254
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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