A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844306



Internal ID22619241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110570161..110584844hg38UCSC Ensembl
chr6:110891364..110906047hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3814684
hg1914684
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500919
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844306
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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