A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089969



Internal ID21999202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27948798..27948798hg38UCSC Ensembl
chr17:26275824..26275824hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17632167
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089969
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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