A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504367



Internal ID20877628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2755834..2793953hg38UCSC Ensembl
chr17:2659128..2697247hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3838120
hg1938120
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184772
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504367
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