A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16992128



Internal ID62198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:827709..831513hg38UCSC Ensembl
chr7:867346..871150hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg383805
hg193805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459667
Supporting Variants
Samples
Known GenesSUN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16992128
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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