A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062775



Internal ID21473598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206924299..206924299hg38UCSC Ensembl
chr1:207097644..207097644hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38506
hg19506
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616980
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062775
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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