A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097201



Internal ID22006434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58966537..58966537hg38UCSC Ensembl
chr17:57043898..57043898hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618303
Samples
Known GenesPPM1E
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097201
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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