A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458751



Internal ID22516634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102829380..102831579hg38UCSC Ensembl
chr13:103481730..103483929hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860468
Supporting Variants
Samples
Known GenesBIVM, BIVM-ERCC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458751
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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