A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766702



Internal ID20542562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150990247..150990247hg38UCSC Ensembl
chr1:150962723..150962723hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263643
Samples
Known GenesANXA9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766702
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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