A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17443276



Internal ID22501146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126145220..126149805hg38UCSC Ensembl
chr9:128907499..128912084hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg384586
hg194586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923012
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17443276
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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