A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16917743



Internal ID12568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:127233717..127239000hg38UCSC Ensembl
chr2:127991293..127996576hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg385284
hg195284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453136
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16917743
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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