A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841780



Internal ID22616715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140704810..140711997hg38UCSC Ensembl
chr5:140084395..140091582hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg387188
hg197188
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495587
Samples
Known GenesVTRNA1-1, ZMAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841780
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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