A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468718



Internal ID21126271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:74764142..74853041hg38UCSC Ensembl
chr12:75157922..75246821hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3888900
hg1988900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003321
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468718
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