A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611758



Internal ID20984829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139278701..139287100hg38UCSC Ensembl
chr6:139599838..139608237hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg388400
hg198400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216872
Samples
Known GenesTXLNB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611758
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