A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466511



Internal ID21124064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30792401..30797700hg38UCSC Ensembl
chr12:30945335..30950634hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998957
Samples
Known GenesLINC00941
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466511
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