A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16992137



Internal ID62206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:876285..877184hg38UCSC Ensembl
chr7:915922..916821hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454380
Supporting Variants
Samples
Known GenesGET4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16992137
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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