A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17006409



Internal ID71899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145011213..145012693hg38UCSC Ensembl
chr7:144708306..144709786hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg381481
hg191481
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489543
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17006409
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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