A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064873



Internal ID21974106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158765833..158765833hg38UCSC Ensembl
chr4:159686985..159686985hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg382677
hg192677
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064873
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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