A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449246



Internal ID21106799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45417564..45580990hg38UCSC Ensembl
chr10:45913012..46076438hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38163427
hg19163427
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184929
Samples
Known GenesALOX5, MARCH8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449246
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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