A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848569



Internal ID22623504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24572707..24575306hg38UCSC Ensembl
chr14:25041913..25044512hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468885, nssv17463551
Samples
Known GenesCTSG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848569
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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