A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844246



Internal ID22619181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119890997..119895363hg38UCSC Ensembl
chr6:120212143..120216509hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg384367
hg194367
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500988
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844246
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