A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5472871



Internal ID250574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:48936318..48936410hg38UCSC Ensembl
chr6:48903955..48904047hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5472871
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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