A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563641



Internal ID336572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:30478183..30483516hg38UCSC Ensembl
chr5:30478290..30483623hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg385334
hg195334
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16964011
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563641
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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