A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399688



Internal ID21057241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39866093..40138119hg38UCSC Ensembl
chr6:39833869..40105858hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38272027
hg19271990
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229421
Samples
Known GenesDAAM2, MOCS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399688
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