A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056181



Internal ID21965414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135846071..135846071hg38UCSC Ensembl
chr2:136603641..136603641hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg381222
hg191222
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531795
Samples
Known GenesMCM6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056181
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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