A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844842



Internal ID22619777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25097922..25099323hg38UCSC Ensembl
chr6:25098150..25099551hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504376, nssv17504377
Samples
Known GenesCMAHP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844842
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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