A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184430



Internal ID20751470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15731001..15774100hg38UCSC Ensembl
chr17:15634315..15677414hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3843100
hg1943100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508865
Supporting Variants
Samples
Known GenesCDRT15P2, TBC1D26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184430
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00671


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