A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929908



Internal ID20678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2151544..2151546hg38UCSC Ensembl
chr3:2193228..2193230hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535140
Supporting Variants
Samples
Known GenesCNTN4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929908
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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