A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661888



Internal ID21610193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1946506..1946506hg38UCSC Ensembl
chr17:1849800..1849800hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090356
SamplesHG00096
Known GenesRTN4RL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661888
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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