A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563564



Internal ID336496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:183146104..183147719hg38UCSC Ensembl
chr1:183115239..183116854hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg381616
hg191616
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16893101
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563564
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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