A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929787



Internal ID20589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:7506064..7759014hg38UCSC Ensembl
chr3:7547751..7800701hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38252951
hg19252951
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436258
Supporting Variants
Samples
Known GenesGRM7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929787
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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