A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062737



Internal ID21971970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:51905800..51905800hg38UCSC Ensembl
chr8:52818360..52818360hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg382397
hg192397
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590644
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062737
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