A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16999547



Internal ID67275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86806779..86828779hg38UCSC Ensembl
chr7:86436095..86458095hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3822001
hg1922001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491988
Supporting Variants
Samples
Known GenesGRM3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16999547
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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