A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971871



Internal ID22746806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61559187..61559187hg38UCSC Ensembl
chr14:62025905..62025905hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379140
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971871
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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