A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840925



Internal ID22615860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10282540..10284689hg38UCSC Ensembl
chr5:10282652..10284801hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg382150
hg192150
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492301
Samples
Known GenesCMBL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840925
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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