A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987860



Internal ID59344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107138510..107138752hg38UCSC Ensembl
chr6:107459714..107459956hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472461
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987860
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.007027


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