A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835389



Internal ID22610324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173647157..173659681hg38UCSC Ensembl
chr3:173364947..173377471hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3812525
hg1912525
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490338
Samples
Known GenesNLGN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835389
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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