A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938395



Internal ID22713774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37105475..37108490hg38UCSC Ensembl
chr13:37679612..37682627hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg383016
hg193016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370634
Samples
Known GenesCSNK1A1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938395
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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