A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081803



Internal ID21991036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10702302..10702302hg38UCSC Ensembl
chr17:10605619..10605619hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17630868
Samples
Known GenesADPRM
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081803
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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