A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886735



Internal ID22661724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8464606..8466905hg38UCSC Ensembl
chr19:8529490..8531789hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480406
Samples
Known GenesHNRNPM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886735
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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