A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600294



Internal ID20973365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132391301..132410600hg38UCSC Ensembl
chr6:132712440..132731739hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3819300
hg1919300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215580
Samples
Known GenesMOXD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600294
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