A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209229



Internal ID20776269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173349589..173448105hg38UCSC Ensembl
chr3:173067379..173165895hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3898517
hg1998517
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374450
Supporting Variants
Samples
Known GenesNLGN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209229
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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