A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17020888



Internal ID81572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21806005..21817449hg38UCSC Ensembl
chr9:21806004..21817448hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3811445
hg1911445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479271
Supporting Variants
Samples
Known GenesMTAP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17020888
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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