A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559790



Internal ID332813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56906741..56909432hg38UCSC Ensembl
chr12:57300525..57303216hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg382692
hg192692
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17057797
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559790
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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