A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436141



Internal ID214763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38758542..38772605hg38UCSC Ensembl
chr2:38985684..38999747hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3814064
hg1914064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16912490
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436141
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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