A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004779



Internal ID70825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149095877..149096412hg38UCSC Ensembl
chr7:148792969..148793504hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476303
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004779
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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