A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936143



Internal ID22711494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106831756..106832578hg38UCSC Ensembl
chr13:107484104..107484926hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38823
hg19823
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364671
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936143
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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