A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190770



Internal ID20757810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64473087..64475386hg38UCSC Ensembl
chr17:62469204..62471503hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525113
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190770
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