A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864994



Internal ID22639929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61136773..61138001hg38UCSC Ensembl
chr14:61603491..61604719hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg381229
hg191229
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465722
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864994
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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