A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606529



Internal ID21798576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48529974..48530078hg38UCSC Ensembl
chr15:48822171..48822275hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020796
Supporting Variants
Samples
Known GenesFBN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606529
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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