A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211436



Internal ID20778476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173910410..173987726hg38UCSC Ensembl
chr3:173628200..173705516hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3877317
hg1977317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360220
Supporting Variants
Samples
Known GenesNLGN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211436
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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