A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459867



Internal ID21117420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:26005085..26062388hg38UCSC Ensembl
chr12:26158018..26215321hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3857304
hg1957304
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194845
Samples
Known GenesRASSF8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459867
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