A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009055



Internal ID21918398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156658658..156666881hg38UCSC Ensembl
chr5:156085669..156093892hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg388224
hg198224
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558201
Samples
Known GenesSGCD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009055
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