A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908898



Internal ID22684108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4567790..4633574hg38UCSC Ensembl
chr7:4607421..4673205hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3865785
hg1965785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439991
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908898
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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