A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6018639



Internal ID21927982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:128445699..128452168hg38UCSC Ensembl
chr6:128766844..128773313hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg386470
hg196470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575599
Samples
Known GenesPTPRK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6018639
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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