A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463708



Internal ID21121261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:84834770..84891534hg38UCSC Ensembl
chr12:85228549..85285313hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3856765
hg1956765
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188406
Samples
Known GenesSLC6A15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463708
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