A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065506



Internal ID21974739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1355787..1355787hg38UCSC Ensembl
chr6:1356022..1356022hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563121
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065506
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