A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561694



Internal ID334664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:245126079..245126125hg38UCSC Ensembl
chr1:245289381..245289427hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3847
hg1947
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16899903
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561694
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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