A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735666



Internal ID159332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46148538..46148960hg38UCSC Ensembl
chr7:46188136..46188558hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475102
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735666
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.010147


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