A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5437049



Internal ID215649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:116813016..116984074hg38UCSC Ensembl
chr3:116531863..116702921hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38171059
hg19171059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv353n206
Supporting Variantsnssv16938647
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5437049
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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