A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558703



Internal ID331760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:60997599..61031576hg38UCSC Ensembl
chr12:61391380..61425357hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3833978
hg1933978
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17059031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558703
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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