A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6086020



Internal ID21995253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78558456..78558456hg38UCSC Ensembl
chr17:76554538..76554538hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621575
Samples
Known GenesDNAH17
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6086020
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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