A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506286



Internal ID20879564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1962496..1969196hg38UCSC Ensembl
chr17:1865790..1872490hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg386701
hg196701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034819
Samples
Known GenesRTN4RL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506286
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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