A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844802



Internal ID22619737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165470209..165471408hg38UCSC Ensembl
chr6:165883697..165884896hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502975, nssv17502976
Samples
Known GenesPDE10A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844802
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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