A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17445432



Internal ID22503302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92058220..92058295hg38UCSC Ensembl
chr9:94820502..94820577hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923080
Supporting Variants
Samples
Known GenesSPTLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17445432
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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