A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936402



Internal ID22711756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31486886..31487074hg38UCSC Ensembl
chr13:32061023..32061211hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383371
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936402
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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