A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519785



Internal ID20893146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63726301..63729400hg38UCSC Ensembl
chr17:61803661..61806760hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191752
Samples
Known GenesSTRADA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519785
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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