A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596974



Internal ID21545584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35561781..35562074hg38UCSC Ensembl
chr17:33888800..33889093hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081850
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596974
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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