A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839615



Internal ID22614550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48417921..48431777hg38UCSC Ensembl
chr4:48419938..48433794hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3813857
hg1913857
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495257
Samples
Known GenesSLAIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839615
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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