A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866740



Internal ID22641675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66957891..66965209hg38UCSC Ensembl
chr7:66422878..66430196hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg387319
hg197319
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508875
Samples
Known GenesTMEM248
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866740
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