A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735729



Internal ID159395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119578347..119593805hg38UCSC Ensembl
chr7:119218401..119233859hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3815459
hg1915459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484658
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735729
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001718


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