A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175824



Internal ID20742864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:22046218..22046800hg38UCSC Ensembl
chr9:22046217..22046799hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433020
Supporting Variants
Samples
Known GenesCDKN2B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175824
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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