A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849883



Internal ID22624818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65152402..65153645hg38UCSC Ensembl
chr14:65619120..65620363hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg381244
hg191244
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462122
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849883
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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