A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739844



Internal ID20515820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67609440..67609556hg38UCSC Ensembl
chr15:67901778..67901894hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296652
Samples
Known GenesMAP2K5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739844
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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