A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352984



Internal ID22578653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103954041..103955313hg38UCSC Ensembl
chr13:104606391..104607663hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg381273
hg191273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5930147
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352984
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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