A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844215



Internal ID22619150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110862639..110865481hg38UCSC Ensembl
chr6:111183842..111186684hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382843
hg192843
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500923
Samples
Known GenesAMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844215
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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