A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559009



Internal ID332057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33821384..33822443hg38UCSC Ensembl
chr13:34395521..34396580hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg381060
hg191060
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686782
Samples
Known GenesRFC3
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559009
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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