A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436951



Internal ID22494821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96300300..96300637hg38UCSC Ensembl
chr9:99062582..99062919hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921969
Supporting Variants
Samples
Known GenesHSD17B3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436951
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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