A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183055



Internal ID20750095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12219496..12266072hg38UCSC Ensembl
chr17:12122813..12169389hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3846577
hg1946577
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508973
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183055
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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