A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5587754



Internal ID21536312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50836475..50836591hg38UCSC Ensembl
chr17:48913836..48913952hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092261
SamplesNA19238
Known GenesWFIKKN2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5587754
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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