A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856496



Internal ID22631431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:133213316..133219315hg38UCSC Ensembl
chr12:133789902..133795901hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg386000
hg196000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451643, nssv17467431
Samples
Known GenesANHX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856496
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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