A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385449



Internal ID22443319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:23232396..24980778hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381748383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935437
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385449
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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