A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855696



Internal ID22630631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:46546951..46548687hg38UCSC Ensembl
chr14:47016154..47017890hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg381737
hg191737
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461668, nssv17451619
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855696
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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