A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362243



Internal ID22587912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104583407..104586384hg38UCSC Ensembl
chr13:105235758..105238735hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg382978
hg192978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936136
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362243
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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