A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844968



Internal ID22619903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44369791..44371172hg38UCSC Ensembl
chr6:44337528..44338909hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381382
hg191382
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505812
Samples
Known GenesSPATS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844968
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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