A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753865



Internal ID20529725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8746826..8746826hg38UCSC Ensembl
chr17:8650144..8650144hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259931
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753865
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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