A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261990



Internal ID20471208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69816450..69816450hg38UCSC Ensembl
chr6:70526342..70526342hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758431
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261990
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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