A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625560



Internal ID21573865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133679993..133679993hg38UCSC Ensembl
chr5:133015684..133015684hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120568
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625560
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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