A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632597



Internal ID21580902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:13427568..13427568hg38UCSC Ensembl
chr5:13427680..13427680hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120563, nssv17136676
SamplesNA18534, HG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632597
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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