A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196724



Internal ID20763764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39637291..39640487hg38UCSC Ensembl
chr17:37793544..37796740hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383197
hg193197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499984
Supporting Variants
Samples
Known GenesSTARD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196724
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