A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5470146



Internal ID247917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27260853..27263104hg38UCSC Ensembl
chr6:27228632..27230883hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg382252
hg192252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16980173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5470146
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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