A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098286



Internal ID22007519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58726544..58726544hg38UCSC Ensembl
chr17:56803905..56803905hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621902
Samples
Known GenesRAD51C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098286
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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