A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071095



Internal ID21980328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51111163..51111163hg38UCSC Ensembl
chr5:50406997..50406997hg19UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551924
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071095
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