A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043472



Internal ID21952776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66431845..66431845hg38UCSC Ensembl
chr2:66658977..66658977hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537189
Samples
Known GenesMEIS1-AS3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043472
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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