A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037190



Internal ID20604230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6268880..6278123hg38UCSC Ensembl
chr17:6172200..6181443hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg389244
hg199244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498908
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037190
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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