A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609611



Internal ID20982682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139271901..139288000hg38UCSC Ensembl
chr6:139593038..139609137hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3816100
hg1916100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216870
Samples
Known GenesTXLNB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609611
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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