A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004473



Internal ID70618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142009758..142009784hg38UCSC Ensembl
chr7:141709558..141709584hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539841
Supporting Variants
Samples
Known GenesMGAM
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004473
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.009522


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