A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17444817



Internal ID22502687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87060413..87068099hg38UCSC Ensembl
chr9:89675328..89683014hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg387687
hg197687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915846
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17444817
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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