A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890272



Internal ID167677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151282587..151288587hg38UCSC Ensembl
chr1:151255063..151261063hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6137946
Supporting Variants
Samples
Known GenesZNF687
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890272
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00411


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