A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551732



Internal ID325163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55539796..55539820hg38UCSC Ensembl
chr7:55607489..55607513hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16998493
Samples
Known GenesVOPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551732
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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