A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514443



Internal ID22572401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81949808..81957290hg38UCSC Ensembl
chr9:84564723..84572205hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg387483
hg197483
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865575
Supporting Variants
Samples
Known GenesSPATA31D3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514443
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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