A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026695



Internal ID21936038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45190014..45190211hg38UCSC Ensembl
chr12:45583797..45583994hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598348
Samples
Known GenesPLEKHA8P1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026695
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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