A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061963



Internal ID21971196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:19817316..19817316hg38UCSC Ensembl
chr4:19818939..19818939hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540040
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061963
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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