A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843807



Internal ID22618742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88688130..88690793hg38UCSC Ensembl
chr5:87983947..87986610hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg382664
hg192664
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499512
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843807
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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