A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861782



Internal ID22636717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:78289540..78304425hg38UCSC Ensembl
chr13:78863675..78878560hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3814886
hg1914886
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460175
Samples
Known GenesRNF219-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861782
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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