A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368667



Internal ID21026220
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 StatusM
Merged Variants
Supporting Variantsnssv18209743
Samples
Known GenesPLCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368667
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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