A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274811



Internal ID20484029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:81998973..81998973hg38UCSC Ensembl
chr1:82464657..82464657hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752107
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274811
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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