A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5570489



Internal ID21518856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108559076..108559164hg38UCSC Ensembl
chr5:107894777..107894865hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120339
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5570489
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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