A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844079



Internal ID22619014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149492315..149507072hg38UCSC Ensembl
chr6:149813451..149828208hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3814758
hg1914758
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501649
Samples
Known GenesPPIL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844079
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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