A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856975



Internal ID22631910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:133199739..133201212hg38UCSC Ensembl
chr12:133776325..133777798hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg381474
hg191474
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459070, nssv17450095
Samples
Known GenesZNF268
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856975
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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