A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471235



Internal ID21128788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:43148452..43148977hg38UCSC Ensembl
chr12:43542255..43542780hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000572
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471235
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer