A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4741277



Internal ID20517254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:410941..411193hg38UCSC Ensembl
chr7:450907..451159hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16274931
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4741277
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