A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5444408



Internal ID222779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11106222..11107275hg38UCSC Ensembl
chr2:11246348..11247401hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381054
hg191054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16909469
Samples
Known GenesFLJ33534
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5444408
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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