A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456926



Internal ID21114479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:73765801..73766600hg38UCSC Ensembl
chr12:74159581..74160380hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003367
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456926
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