A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439150



Internal ID22497020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97069193..97069539hg38UCSC Ensembl
chr9:99831475..99831821hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927386
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439150
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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