A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004786



Internal ID70830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149123692..149129008hg38UCSC Ensembl
chr7:148820784..148826100hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg385317
hg195317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482542
Supporting Variants
Samples
Known GenesZNF398, ZNF425
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004786
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003125


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