A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022646



Internal ID82784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74086765..74089718hg38UCSC Ensembl
chr9:76701681..76704634hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382954
hg192954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486865
Supporting Variants
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022646
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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