A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034793



Internal ID20601833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1948936..1965244hg38UCSC Ensembl
chr17:1852230..1868538hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3816309
hg1916309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495906
Supporting Variants
Samples
Known GenesRTN4RL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034793
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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