A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275779



Internal ID20484997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60682418..60682418hg38UCSC Ensembl
chr11:60449891..60449891hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38958
hg19958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754717
Supporting Variants
Samples
Known GenesLINC00301
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275779
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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