A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468991



Internal ID22526881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100311475..100318614hg38UCSC Ensembl
chr13:100963729..100970868hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg387140
hg197140
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863173
Supporting Variants
Samples
Known GenesPCCA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468991
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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