A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003604



Internal ID21912947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158206615..158229116hg38UCSC Ensembl
chr6:158627647..158650148hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3822502
hg1922502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575765
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003604
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