A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469892



Internal ID247667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150493648..150494125hg38UCSC Ensembl
chr5:149873210..149873687hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974779
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469892
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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