A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977928



Internal ID52689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:185635..185686hg38UCSC Ensembl
chr6:185635..185686hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5537122
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977928
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.052451


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