A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270600



Internal ID20479818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127074253..127074253hg38UCSC Ensembl
chr8:128086498..128086498hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756590
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270600
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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