A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865247



Internal ID22640182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49549252..49562576hg38UCSC Ensembl
chr13:50123388..50136712hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg3813325
hg1913325
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455913
Samples
Known GenesRCBTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865247
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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