A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532877



Internal ID308789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45026600..45032874hg38UCSC Ensembl
chr15:45318798..45325072hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg386275
hg196275
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701648
Samples
Known GenesSORD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532877
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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