A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754726



Internal ID20530586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78351205..78351205hg38UCSC Ensembl
chr17:76347286..76347286hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38516
hg19516
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276626
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754726
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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