A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412238



Internal ID21069791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14264839..14265817hg38UCSC Ensembl
chr6:14265070..14266048hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38979
hg19979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140171
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412238
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