A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17003676



Internal ID70076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135171096..135171315hg38UCSC Ensembl
chr7:134855848..134856067hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477222
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17003676
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001093


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