A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869289



Internal ID22644224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:346286..349279hg38UCSC Ensembl
chr20:326930..329923hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382994
hg192994
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485319
Samples
Known GenesNRSN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869289
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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