A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935021



Internal ID22710356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32415531..32415676hg38UCSC Ensembl
chr13:32989668..32989813hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377961
Samples
Known GenesN4BP2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935021
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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