A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760036



Internal ID20535896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70312993..70312993hg38UCSC Ensembl
chr17:68309134..68309134hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760036
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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