A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622669



Internal ID21570974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10873409..10873409hg38UCSC Ensembl
chr3:10915094..10915094hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123131
SamplesHG00732
Known GenesSLC6A11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622669
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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