A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978035



Internal ID52760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3608151..3608201hg38UCSC Ensembl
chr6:3608385..3608435hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538882
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978035
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.099888


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