A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073316



Internal ID21982549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185125358..185125358hg38UCSC Ensembl
chr4:186046512..186046512hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548632
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073316
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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