A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16995365



Internal ID64337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:49235267..49245495hg38UCSC Ensembl
chr7:49274863..49285091hg19UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg3810229
hg1910229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489809
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16995365
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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