A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863008



Internal ID22637943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18179226..18180523hg38UCSC Ensembl
chrUn_gl000212:7978..9275hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381298
hg191298
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454874, nssv17467357, nssv17461601
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863008
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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