A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496418



Internal ID20869620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1946491..1946846hg38UCSC Ensembl
chr17:1849785..1850140hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192895
Samples
Known GenesRTN4RL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496418
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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