A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438749



Internal ID22496619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33423085..33424832hg38UCSC Ensembl
chr9:33423083..33424830hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381748
hg191748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5919628
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438749
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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