A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848936



Internal ID22623871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94446742..94485987hg38UCSC Ensembl
chr14:94913079..94952324hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3839246
hg1939246
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470372
Samples
Known GenesSERPINA11, SERPINA9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848936
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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