A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757893



Internal ID20533753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34686891..34686891hg38UCSC Ensembl
chr6:34654668..34654668hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273096
Samples
Known GenesC6orf106
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757893
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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