A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061523



Internal ID21970756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101623751..101623751hg38UCSC Ensembl
chr8:102635979..102635979hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578256
Samples
Known GenesGRHL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061523
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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