A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5598824



Internal ID21547453
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 StatusM
Merged Variants
Supporting Variantsnssv17163170
SamplesNA19983
Known GenesSLC35D2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5598824
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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