A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385354



Internal ID22443224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43995318..43995746hg38UCSC Ensembl
chr13:44569454..44569882hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929320
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385354
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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