A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456726



Internal ID22514605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:61043644..61046906hg38UCSC Ensembl
chr13:61617778..61621040hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg383263
hg193263
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848176
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456726
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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