A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023176



Internal ID83172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68676213..68721185hg38UCSC Ensembl
chr9:71291129..71336101hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3844973
hg1944973
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487169
Supporting Variants
Samples
Known GenesPIP5K1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023176
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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