A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871449



Internal ID22646387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19522514..19524731hg38UCSC Ensembl
chr19:19633323..19635540hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg382218
hg192218
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473877
Samples
Known GenesNDUFA13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871449
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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