A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068741



Internal ID21977974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141502241..141502241hg38UCSC Ensembl
chr7:141202041..141202041hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg382449
hg192449
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560547
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068741
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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