A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6039420



Internal ID21948763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:96338571..96338983hg38UCSC Ensembl
chr12:96732349..96732761hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612498
Samples
Known GenesCDK17
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6039420
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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