A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761490



Internal ID20537350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63177371..63177371hg38UCSC Ensembl
chr1:63643042..63643042hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291260
Samples
Known GenesLINC00466
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761490
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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