A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458616



Internal ID22516499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27872536..27877270hg38UCSC Ensembl
chr13:28446673..28451407hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg384735
hg194735
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848201
Supporting Variants
Samples
Known GenesPDX1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458616
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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