A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943198



Internal ID22718643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112014887..112015174hg38UCSC Ensembl
chr13:112669201..112669488hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368606
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943198
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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