A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456680



Internal ID234741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101567812..101578997hg38UCSC Ensembl
chr6:102015687..102026872hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3811186
hg1911186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16988561
Samples
Known GenesGRIK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456680
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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