A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559528



Internal ID332560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78327401..78585274hg38UCSC Ensembl
chr3:78376551..78634424hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38257874
hg19257874
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16934318
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559528
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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