A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861523



Internal ID22636458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95779612..95781242hg38UCSC Ensembl
chr14:96245949..96247579hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg381631
hg191631
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470199, nssv17470390
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861523
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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