A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839009



Internal ID22613944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39612501..39617338hg38UCSC Ensembl
chr4:39614121..39618958hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg384838
hg194838
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494510
Samples
Known GenesSMIM14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839009
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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