A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5592463



Internal ID21541045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37678362..37678412hg38UCSC Ensembl
chr17:36038366..36038416hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097775
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5592463
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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