A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890876



Internal ID168091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155614000..155750587hg38UCSC Ensembl
chr1:155583791..155720378hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38136588
hg19136588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138228
Supporting Variants
Samples
Known GenesDAP3, GON4L, MSTO1, MSTO2P, YY1AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890876
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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