A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16993152



Internal ID62890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18541272..18542076hg38UCSC Ensembl
chr7:18580895..18581699hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38805
hg19805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456372
Supporting Variants
Samples
Known GenesHDAC9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16993152
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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