A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16286150



Internal ID20495368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24648915..24648915hg38UCSC Ensembl
chr6:24649143..24649143hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751046
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16286150
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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