A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501966



Internal ID278847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100754385..100764995hg38UCSC Ensembl
chr13:101406639..101417249hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3810611
hg1910611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17691224
Samples
Known GenesNALCN-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501966
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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