A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881369



Internal ID22656344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8447157..8460705hg38UCSC Ensembl
chr19:8512041..8525589hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3813549
hg1913549
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480011
Samples
Known GenesHNRNPM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881369
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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