A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765689



Internal ID20541549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20225558..20225558hg38UCSC Ensembl
chr9:20225556..20225556hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270219
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765689
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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