A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876195



Internal ID22651155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1953986..1955120hg38UCSC Ensembl
chr17:1857280..1858414hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg381135
hg191135
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476147, nssv17476148
Samples
Known GenesRTN4RL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876195
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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