A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842729



Internal ID22617664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43101266..43107710hg38UCSC Ensembl
chr5:43101368..43107812hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg386445
hg196445
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496724
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842729
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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