A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042375



Internal ID21951692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:190929125..190929125hg38UCSC Ensembl
chr2:191793851..191793851hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518763
Samples
Known GenesGLS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042375
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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