A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5441918



Internal ID220365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:196448975..196452818hg38UCSC Ensembl
chr2:197313699..197317542hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg383844
hg193844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16923386
Samples
Known GenesHECW2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5441918
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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