A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849896



Internal ID22624831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:133235783..133240818hg38UCSC Ensembl
chr12:133812369..133817404hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg385036
hg195036
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462963, nssv17452155
Samples
Known GenesANHX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849896
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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