A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848901



Internal ID22623836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:78628825..78634409hg38UCSC Ensembl
chr13:79202960..79208544hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg385585
hg195585
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463884
Samples
Known GenesRNF219
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848901
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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