A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154532



Internal ID21484282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16791442..16791442hg38UCSC Ensembl
chr6:16791673..16791673hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632870
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154532
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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