A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065135



Internal ID21974368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:81805079..81805079hg38UCSC Ensembl
chr5:81100898..81100898hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541508
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065135
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