A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602134



Internal ID21550789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25309792..25309850hg38UCSC Ensembl
chr13:25883930..25883988hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092286
SamplesNA19238
Known GenesNUPL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602134
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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