A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401838



Internal ID21059391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88700444..88710022hg38UCSC Ensembl
chr6:89410163..89419741hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg389579
hg199579
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226851
Samples
Known GenesRNGTT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401838
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