A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741577



Internal ID20517554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43293736..43293803hg38UCSC Ensembl
chr15:43585934..43586001hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296022
Samples
Known GenesTGM7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741577
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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