A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17163170



Internal ID21506948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96350297..96350361hg38UCSC Ensembl
chr9:99112579..99112643hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598824
Supporting Variants
SamplesNA19983
Known GenesSLC35D2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17163170
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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