A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513293



Internal ID20886636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66562801..66569000hg38UCSC Ensembl
chr16:66596704..66602903hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180173
Samples
Known GenesCKLF, CKLF-CMTM1, CMTM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513293
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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