A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843588



Internal ID22618523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94803579..94806536hg38UCSC Ensembl
chr5:94139284..94142241hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg382958
hg192958
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499579
Samples
Known GenesMCTP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843588
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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