A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468338



Internal ID22526227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:64951456..64956264hg38UCSC Ensembl
chr13:65525588..65530396hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg384809
hg194809
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5865933
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468338
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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