A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650476



Internal ID21598781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36994603..36994603hg38UCSC Ensembl
chr13:37568740..37568740hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087988
SamplesNA19238
Known GenesALG5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650476
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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