A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000594



Internal ID21909937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21677724..23021905hg38UCSC Ensembl
chr9:21677723..23021904hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg381344182
hg191344182
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591818
Samples
Known GenesC9orf53, CDKN2A, CDKN2B, CDKN2B-AS1, DMRTA1, FLJ35282, MTAP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000594
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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