A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019065



Internal ID21928408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131175909..131177483hg38UCSC Ensembl
chr7:130860668..130862242hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg381575
hg191575
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565796
Samples
Known GenesMKLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019065
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