A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17003657



Internal ID70064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135001394..135011662hg38UCSC Ensembl
chr7:134686145..134696413hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3810269
hg1910269
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475643
Supporting Variants
Samples
Known GenesAGBL3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17003657
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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