A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033685



Internal ID21943028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:54906694..54938145hg38UCSC Ensembl
chr12:55300478..55331929hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg3831452
hg1931452
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033685
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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