A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004776



Internal ID70822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149073793..149073804hg38UCSC Ensembl
chr7:148770885..148770896hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541706
Supporting Variants
Samples
Known GenesZNF786
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004776
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002029


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