A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556562



Internal ID329698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109088504..109088576hg38UCSC Ensembl
chr1:109631126..109631198hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16908837
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556562
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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