A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071278



Internal ID21980511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153021756..153021756hg38UCSC Ensembl
chr6:153342891..153342891hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574367
Samples
Known GenesRGS17
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071278
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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