A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468236



Internal ID22526125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:92115852..92132282hg38UCSC Ensembl
chr13:92768105..92784535hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3816431
hg1916431
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866772
Supporting Variants
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468236
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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