A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844746



Internal ID22619681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149732789..149735315hg38UCSC Ensembl
chr6:150053925..150056451hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg382527
hg192527
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1801n209
Supporting Variantsnssv17502411
Samples
Known GenesNUP43
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844746
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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