A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081052



Internal ID21990285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13368823..13368823hg38UCSC Ensembl
chr17:13272140..13272140hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081052
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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