A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068516



Internal ID21977749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151430881..151430881hg38UCSC Ensembl
chr6:151752016..151752016hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576042
Samples
Known GenesRMND1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068516
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