A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495060



Internal ID21152613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112965771..112968583hg38UCSC Ensembl
chr12:113403576..113406388hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg382813
hg192813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996830
Samples
Known GenesOAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495060
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