A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062689



Internal ID21491602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:216025382..216025382hg38UCSC Ensembl
chr1:216198724..216198724hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5606247
Supporting Variants
SamplesNA19238
Known GenesUSH2A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062689
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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