A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5470373



Internal ID248134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43138068..43138299hg38UCSC Ensembl
chr6:43105806..43106037hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16981658
Samples
Known GenesPTK7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5470373
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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