A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514708



Internal ID22572667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:8858130..8859477hg38UCSC Ensembl
chr9:8858130..8859477hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381348
hg191348
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852153
Supporting Variants
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514708
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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