A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632459



Internal ID21580764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173186068..173186068hg38UCSC Ensembl
chr5:172613071..172613071hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135822
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632459
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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