A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209743



Internal ID20776784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155651095..155760626hg38UCSC Ensembl
chr3:155368884..155478415hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38109532
hg19109532
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368667
Supporting Variants
Samples
Known GenesPLCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209743
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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