A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287291



Internal ID20496509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159604778..159604778hg38UCSC Ensembl
chr6:160025810..160025810hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758257
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287291
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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