A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090343



Internal ID21506308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62907120..62907120hg38UCSC Ensembl
chr17:60984481..60984481hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658740
Supporting Variants
SamplesNA19983
Known GenesMIR548W
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090343
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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