A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17002835



Internal ID69509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96509788..96511930hg38UCSC Ensembl
chr7:96139100..96141242hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg382143
hg192143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476753
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17002835
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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