A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17447327



Internal ID22505197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95680940..95681021hg38UCSC Ensembl
chr9:98443222..98443303hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914324
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17447327
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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