A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733801



Internal ID157467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:6984850..6990000hg38UCSC Ensembl
chr7_gl000195_random:145736..150778hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg385151
hg195043
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146612
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733801
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000838


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