A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513591



Internal ID22571546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43117122..43121736hg38UCSC Ensembl
chr9:42863517..42868135hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg384615
hg194619
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863027
Supporting Variants
Samples
Known GenesAQP7P3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513591
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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