A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461758



Internal ID22519643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:78392410..78394309hg38UCSC Ensembl
chr13:78966545..78968444hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857494
Supporting Variants
Samples
Known GenesRNF219-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461758
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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