A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840928



Internal ID22615863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102945201..102946464hg38UCSC Ensembl
chr5:102280905..102282168hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg381264
hg191264
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17492310
Samples
Known GenesPAM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840928
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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