A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145961



Internal ID345166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4627615..4627908hg38UCSC Ensembl
chr16:4677616..4677909hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704821
Samples
Known GenesMGRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145961
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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