A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073047



Internal ID21982280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112573215..112573215hg38UCSC Ensembl
chr6:112894417..112894417hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073047
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