A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5448976



Internal ID227226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155848047..155848115hg38UCSC Ensembl
chr3:155565836..155565904hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16942209
Samples
Known GenesSLC33A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5448976
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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