A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278136



Internal ID20487354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37774863..37774863hg38UCSC Ensembl
chr6:37742639..37742639hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278136
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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