A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412232



Internal ID21069785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1024966..1034846hg38UCSC Ensembl
chr6:1025201..1035081hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg389881
hg199881
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216500
Samples
Known GenesLOC285768
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412232
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