A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740708



Internal ID20516685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48529859..48530023hg38UCSC Ensembl
chr15:48822056..48822220hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275496
Samples
Known GenesFBN1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740708
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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