A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568019



Internal ID21516362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17293610..17298822hg38UCSC Ensembl
chr5:17293719..17298931hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg385213
hg195213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122088
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568019
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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