A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925632



Internal ID22700859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140481786..140489419hg38UCSC Ensembl
chr7:140181586..140189219hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg387634
hg197634
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925632
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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