A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513598



Internal ID22571553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:43124706..43128288hg38UCSC Ensembl
chr9:42856960..42860525hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg383583
hg193566
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866969
Supporting Variants
Samples
Known GenesAQP7P3, LOC286297
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513598
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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