A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17432306



Internal ID22490176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81545796..81553572hg38UCSC Ensembl
chr9:84160711..84168487hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg387777
hg197777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918649
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17432306
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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