A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633976



Internal ID21582281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176962494..176962494hg38UCSC Ensembl
chr5:176389495..176389495hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136710
SamplesNA19238
Known GenesUIMC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633976
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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