A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5571897



Internal ID21520280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154583474..154583538hg38UCSC Ensembl
chr5:153963034..153963098hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17136959
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5571897
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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