A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865496



Internal ID22640431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38946867..38953218hg38UCSC Ensembl
chr14:39416071..39422422hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg386352
hg196352
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865496
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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