A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856027



Internal ID22630962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:42522079..42524878hg38UCSC Ensembl
chr12:42915881..42918680hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451659
Samples
Known GenesPRICKLE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856027
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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