A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024982



Internal ID84385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91221676..91221817hg38UCSC Ensembl
chr9:93983958..93984099hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487036
Supporting Variants
Samples
Known GenesAUH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024982
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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