A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641659



Internal ID21589964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110473739..110473739hg38UCSC Ensembl
chr6:110794942..110794942hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150081
SamplesHG00512
Known GenesSLC22A16
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641659
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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