A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17005360



Internal ID71193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155218483..155218483hg38UCSC Ensembl
chr7:155010193..155010193hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536299
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17005360
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000313


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