A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5842527



Internal ID22617462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18537151..18541896hg38UCSC Ensembl
chr5:18537260..18542005hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg384746
hg194746
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495085, nssv17495084
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5842527
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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