A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16999546



Internal ID67274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:86803689..86803901hg38UCSC Ensembl
chr7:86433005..86433217hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477144
Supporting Variants
Samples
Known GenesGRM3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16999546
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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