A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065043



Internal ID21974276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113961040..113961040hg38UCSC Ensembl
chr6:114282204..114282204hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575242
Samples
Known GenesHDAC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065043
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