A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436190



Internal ID214811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:73761763..73762887hg38UCSC Ensembl
chr2:73988890..73990014hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg381125
hg191125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16915479
Samples
Known GenesDUSP11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436190
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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