A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442457



Internal ID22500327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126903464..126909465hg38UCSC Ensembl
chr9:129665743..129671744hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg386002
hg196002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922858
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442457
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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