A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936903



Internal ID22712264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132943180..133182732hg38UCSC Ensembl
chr12:133519766..133759318hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38239553
hg19239553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356535
Samples
Known GenesZNF10, ZNF140, ZNF26, ZNF268, ZNF605, ZNF84, ZNF891
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936903
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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