A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146190



Internal ID345395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:74515523..74516422hg38UCSC Ensembl
chr16:74549421..74550320hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708249
Samples
Known GenesGLG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146190
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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