A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844961



Internal ID22619896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42495196..42501207hg38UCSC Ensembl
chr6:42462934..42468945hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg386012
hg196012
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505781
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844961
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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