A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350511



Internal ID22576180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111475199..111475334hg38UCSC Ensembl
chr13:112127546..112127681hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5940447
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350511
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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