A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491661



Internal ID268894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148966160..148966335hg38UCSC Ensembl
chr7:148663252..148663427hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17005661
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491661
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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