A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065796



Internal ID21975029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:114143124..114143124hg38UCSC Ensembl
chr6:114464288..114464288hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561061
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065796
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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