A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764211



Internal ID20540071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60551976..60551976hg38UCSC Ensembl
chr17:58629337..58629337hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764211
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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