A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850718



Internal ID22625653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94515829..94521648hg38UCSC Ensembl
chr14:94982166..94987985hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg385820
hg195820
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470148, nssv17470147
Samples
Known GenesSERPINA12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850718
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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