A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5599768



Internal ID21548405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62462836..62463453hg38UCSC Ensembl
chr17:60540197..60540814hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079700
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5599768
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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