A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946194



Internal ID22721681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67780558..67791708hg38UCSC Ensembl
chr13:68354690..68365840hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3811151
hg1911151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374282
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946194
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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