A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451985



Internal ID22509857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106109023..106110150hg38UCSC Ensembl
chr13:106761372..106762499hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg381128
hg191128
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866603
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451985
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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