A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416931



Internal ID21074484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:22030101..22031300hg38UCSC Ensembl
chr9:22030100..22031299hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175822
Samples
Known GenesCDKN2B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416931
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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