A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004563



Internal ID70673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145306268..145321761hg38UCSC Ensembl
chr7:145003361..145018854hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3815494
hg1915494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492714
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004563
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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