A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633866



Internal ID21582171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135670708..135670708hg38UCSC Ensembl
chr7:135355456..135355456hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139927
SamplesHG03125
Known GenesC7orf73
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633866
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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