A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844041



Internal ID22618976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137062146..137070304hg38UCSC Ensembl
chr6:137383283..137391441hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg388159
hg198159
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501756
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844041
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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