A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13692873



Internal ID21214726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74987682..74988025hg38UCSC Ensembl
chr13:75561819..75562162hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2792751
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13692873
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.359375


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