A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730702



Internal ID20506615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66469118..66471494hg38UCSC Ensembl
chr15:66761456..66763832hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382377
hg192377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292735
Samples
Known GenesMAP2K1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730702
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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