A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027539



Internal ID86064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97138555..97141974hg38UCSC Ensembl
chr9:99900837..99904256hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg383420
hg193420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490377
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027539
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.022011


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