A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514838



Internal ID22572797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94062695..94068739hg38UCSC Ensembl
chr9:96824977..96831021hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg386045
hg196045
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5862035
Supporting Variants
Samples
Known GenesPTPDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514838
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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