A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594649



Internal ID21543249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100754385..100764994hg38UCSC Ensembl
chr13:101406639..101417248hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3810610
hg1910610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095147
SamplesHG03065
Known GenesNALCN-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594649
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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