A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162106



Internal ID21452450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60968150..60968808hg38UCSC Ensembl
chr9:41554422..41555080hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594465
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162106
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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