A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18002655



Internal ID20569695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:67633879..67641068hg38UCSC Ensembl
chr12:68027659..68034848hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg387190
hg197190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462659
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18002655
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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