A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504592



Internal ID20877854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38639246..38640822hg38UCSC Ensembl
chr17:36795499..36797075hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381577
hg191577
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178508
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504592
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