A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848212



Internal ID22623147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:5563501..5567673hg38UCSC Ensembl
chr12:5672667..5676839hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg384173
hg194173
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452493
Samples
Known GenesANO2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848212
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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