A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092261



Internal ID21491974
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 StatusS
Merged Variantsnsv5587754
Supporting Variants
SamplesNA19238
Known GenesWFIKKN2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092261
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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