A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17132883



Internal ID21510990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143631224..143631224hg38UCSC Ensembl
chr5:143010789..143010789hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632691
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17132883
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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