A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068549



Internal ID21977782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:29904073..29904073hg38UCSC Ensembl
chr4:29905695..29905695hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068549
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer