A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843589



Internal ID22618524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95144558..95151932hg38UCSC Ensembl
chr5:94480262..94487636hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg387375
hg197375
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500114
Samples
Known GenesMCTP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843589
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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