A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860610



Internal ID22635545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109490..121546hg38UCSC Ensembl
chr12:218656..230712hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3812057
hg1912057
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457413
Samples
Known GenesIQSEC3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860610
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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