A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182069



Internal ID20749109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21100119..21114358hg38UCSC Ensembl
chr17:21003432..21017671hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3814240
hg1914240
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507140
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182069
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00138


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