A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064841



Internal ID21974074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37037117..37037117hg38UCSC Ensembl
chr4:37038739..37038739hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554165
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064841
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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