A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844321



Internal ID22619256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116547604..116558603hg38UCSC Ensembl
chr6:116868767..116879766hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg3811000
hg1911000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501091
Samples
Known GenesFAM26D
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844321
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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