A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838211



Internal ID22613146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185309071..185313125hg38UCSC Ensembl
chr4:186230225..186234279hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg384055
hg194055
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491368
Samples
Known GenesSNX25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838211
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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