A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517861



Internal ID20891222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:46785037..46787201hg38UCSC Ensembl
chr17:44862403..44864567hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382165
hg192165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192851
Samples
Known GenesWNT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517861
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