A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556212



Internal ID329353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:33091853..33097520hg38UCSC Ensembl
chr12:33244787..33250454hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg385668
hg195668
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17057480
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556212
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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