A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628177



Internal ID21576482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:171473731..171473731hg38UCSC Ensembl
chr5:170900735..170900735hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132986
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628177
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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