A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086776



Internal ID21996009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17252410..17252410hg38UCSC Ensembl
chr17:17155724..17155724hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622323
Samples
Known GenesCOPS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086776
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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