A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291260



Internal ID20500478
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 StatusS
Merged Variantsnsv4761490
Supporting Variants
Samples
Known GenesLINC00466
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291260
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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