A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459265



Internal ID21116818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8209801..8251500hg38UCSC Ensembl
chr12:8362397..8404096hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3841700
hg1941700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1384n223
Supporting Variantsnssv18177347
Samples
Known GenesFAM86FP, FAM90A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459265
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