A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025894



Internal ID85003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65697191..65722000hg38UCSC Ensembl
chr9:42678111..42702920hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3824810
hg1924810
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433092
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025894
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.473404


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