A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641677



Internal ID21589982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159650273..159650273hg38UCSC Ensembl
chr5:159077280..159077280hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122462
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641677
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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