A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840926



Internal ID22615861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102865501..102872061hg38UCSC Ensembl
chr5:102201205..102207765hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg386561
hg196561
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492304, nssv17499305
Samples
Known GenesPAM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840926
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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