A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839648



Internal ID22614583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46803090..46804489hg38UCSC Ensembl
chr4:46805107..46806506hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495247
Samples
Known GenesCOX7B2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839648
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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