A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442523



Internal ID22500393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78180759..78186579hg38UCSC Ensembl
chr9:80795675..80801495hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg385821
hg195821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924389
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442523
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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