A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840612



Internal ID22615547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:105941649..105942948hg38UCSC Ensembl
chr5:105277350..105278649hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840612
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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