A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091956



Internal ID22001189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75982702..75982702hg38UCSC Ensembl
chr17:73978783..73978783hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620001
Samples
Known GenesTEN1, TEN1-CDK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091956
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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