A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561277



Internal ID334261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157616186..157622741hg38UCSC Ensembl
chr1:157585976..157592531hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg386556
hg196556
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16890985
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561277
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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