A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17005166



Internal ID71071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128386613..128386613hg38UCSC Ensembl
chr7:128026667..128026667hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5545364
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17005166
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003916


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