A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936182



Internal ID22711533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51551667..51552631hg38UCSC Ensembl
chr13:52125803..52126767hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38965
hg19965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372040
Samples
Known GenesMIR4703
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936182
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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