A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437770



Internal ID216353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206008547..206025186hg38UCSC Ensembl
chr1:206316182..206332221hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3816640
hg1916040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16895271
Samples
Known GenesCTSE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437770
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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