A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867063



Internal ID22641998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57353259..57355312hg38UCSC Ensembl
chr12:57747042..57749095hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg382054
hg192054
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv416n209
Supporting Variantsnssv17466729
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867063
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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