A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5642592



Internal ID21590897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151166574..151166574hg38UCSC Ensembl
chr5:150546135..150546135hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg382472
hg192472
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123579
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5642592
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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