A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068632



Internal ID21977865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150784568..150784568hg38UCSC Ensembl
chr5:150164130..150164130hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561705
Samples
Known GenesSMIM3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068632
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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