A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031012



Internal ID21940355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10651040..10651127hg38UCSC Ensembl
chr17:10554357..10554444hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17635960
Samples
Known GenesMYH3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031012
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer