A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924951



Internal ID22700178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155613121..155621973hg38UCSC Ensembl
chr7:155405815..155414667hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg388853
hg198853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924951
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