A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16906753



Internal ID5285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98409815..98805656hg38UCSC Ensembl
chr1:98875371..99271212hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38395842
hg19395842
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431010
Supporting Variants
Samples
Known GenesSNX7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16906753
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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