A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16981399



Internal ID54969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43776465..43776774hg38UCSC Ensembl
chr6:43744202..43744511hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458096
Supporting Variants
Samples
Known GenesVEGFA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16981399
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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