A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844633



Internal ID22619568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143105303..143110353hg38UCSC Ensembl
chr6:143426440..143431490hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg385051
hg195051
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501830
Samples
Known GenesAIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844633
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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