A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733925



Internal ID20509857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38717696..38719932hg38UCSC Ensembl
chr2:38944838..38947074hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg382237
hg192237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293778
Samples
Known GenesGALM
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733925
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer