A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17448854



Internal ID22506724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:106309101..106313960hg38UCSC Ensembl
chr9:109071382..109076241hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg384860
hg194860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927473
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17448854
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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