A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866768



Internal ID22641703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118970256..118976633hg38UCSC Ensembl
chr12:119408061..119414438hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg386378
hg196378
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453448
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866768
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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