A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844475



Internal ID22619410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168472206..168476801hg38UCSC Ensembl
chr6:168872886..168877481hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg384596
hg194596
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503053
Samples
Known GenesSMOC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844475
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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