A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067371



Internal ID21976604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170046192..170046192hg38UCSC Ensembl
chr4:170967343..170967343hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549447
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067371
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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