A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190029



Internal ID20757069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81667584..81671280hg38UCSC Ensembl
chr17:79634614..79638310hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg383697
hg193697
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526615
Supporting Variants
Samples
Known GenesCCDC137
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190029
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