A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853960



Internal ID22628895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67771359..67773422hg38UCSC Ensembl
chr7:67236346..67238409hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg382064
hg192064
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853960
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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