A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766521



Internal ID20542381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111123805..111123805hg38UCSC Ensembl
chr1:111666427..111666427hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg381122
hg191122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265411
Samples
Known GenesDRAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766521
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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