A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099746



Internal ID22008979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7683541..7683541hg38UCSC Ensembl
chr17:7586859..7586859hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622016
Samples
Known GenesTP53
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099746
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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