A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908210



Internal ID6268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85676764..85676831hg38UCSC Ensembl
chr1:86142447..86142514hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426376
Supporting Variants
Samples
Known GenesZNHIT6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908210
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001093


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