A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467669



Internal ID245479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41283781..41290119hg38UCSC Ensembl
chr6:41251519..41257857hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg386339
hg196339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16983140
Samples
Known GenesTREM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467669
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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