A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627059



Internal ID21575364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157883434..157883434hg38UCSC Ensembl
chr5:157310442..157310442hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124700
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627059
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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