A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461748



Internal ID22519633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:97150742..97156312hg38UCSC Ensembl
chr13:97802996..97808566hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg385571
hg195571
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856725
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461748
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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