A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456224



Internal ID22514101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100276711..100277910hg38UCSC Ensembl
chr13:100928965..100930164hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853962
Supporting Variants
Samples
Known GenesPCCA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456224
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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