A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608101



Internal ID20981172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145825679..145863042hg38UCSC Ensembl
chr6:146146815..146184178hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3837364
hg1937364
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216952
Samples
Known GenesLOC100507557
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608101
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