A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16997631



Internal ID65965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66162048..66174149hg38UCSC Ensembl
chr7:65627035..65639136hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3812102
hg1912102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478064
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16997631
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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