A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020875



Internal ID21930218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67609444..67609503hg38UCSC Ensembl
chr15:67901782..67901841hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606953
Samples
Known GenesMAP2K5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020875
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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