A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437676



Internal ID216261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52434600..52434900hg38UCSC Ensembl
chr3:52468616..52468916hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932759
Samples
Known GenesSEMA3G
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437676
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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