A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17004594



Internal ID70697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145610227..145612960hg38UCSC Ensembl
chr7:145307320..145310053hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg382734
hg192734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479265
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17004594
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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