A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528548



Internal ID304600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49358874..49400937hg38UCSC Ensembl
chr15:49651071..49693134hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3842064
hg1942064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703038
Samples
Known GenesFAM227B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528548
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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