A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17005255



Internal ID71132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132016079..132018380hg38UCSC Ensembl
chr7:131700838..131703139hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg382302
hg192302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477178
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17005255
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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