A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577026



Internal ID21525472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117358812..117359135hg38UCSC Ensembl
chr5:116694508..116694831hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120617
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577026
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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