A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748266



Internal ID20524291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75603465..75603552hg38UCSC Ensembl
chr15:75895806..75895893hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289694
Samples
Known GenesSNUPN
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748266
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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