A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036777



Internal ID20603817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:54755622..54827574hg38UCSC Ensembl
chr17:52832983..52904935hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3871953
hg1971953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522355
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036777
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