A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979014



Internal ID53386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11308231..11308383hg38UCSC Ensembl
chr6:11308464..11308616hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462295
Supporting Variants
Samples
Known GenesNEDD9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979014
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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