A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936621



Internal ID22711978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33205230..33217138hg38UCSC Ensembl
chr19:33696136..33708044hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3811909
hg1911909
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390626
Samples
Known GenesLRP3, SLC7A10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936621
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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