A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17129071



Internal ID21468441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:4973415..4973415hg38UCSC Ensembl
chr5:4973528..4973528hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5637488
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17129071
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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