A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433194



Internal ID22491064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32285804..32291331hg38UCSC Ensembl
chr9:32285802..32291329hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg385528
hg195528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5916077
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433194
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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