A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007652



Internal ID21916995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100190711..100190917hg38UCSC Ensembl
chr8:101202939..101203145hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595691
Samples
Known GenesSPAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007652
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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